{
  "id": "synjardy-xr",
  "recordTier": "source_traceable_archive",
  "editorial": {
    "reviewedAt": "2026-08-30",
    "status": "published_traceable_archive"
  },
  "names": {
    "brand": "SYNJARDY XR",
    "generic": "恩格列净/盐酸二甲双胍缓释片",
    "aliases": [
      "Synjardy XR",
      "empagliflozin and metformin hydrochloride extended-release",
      "empagliflozin metformin XR",
      "恩格列净二甲双胍缓释片",
      "恩格列净/盐酸二甲双胍缓释片",
      "empagliflozin and metformin hydrochloride",
      "NDA 208658",
      "0597-0280-73",
      "0597-0290-74",
      "0597-0295-88",
      "0597-0300-45",
      "S10 1000",
      "S5 1000",
      "S25 1000",
      "S12 1000"
    ],
    "marketBrandNames": [],
    "mainlandChinaTradeNameCue": null
  },
  "identity": {
    "therapeuticArea": "代谢",
    "sourceArchiveMarket": "美国 SYNJARDY XR 当前 DailyMed 公开品牌标签（SPL v18；2026-08-11 更新，2026-08-21 发布；NDA 208658）。本档案精确建立标签展示的四种代表性瓶装面板；另四个在标签包装表中列出的瓶装 NDC 不由没有对应展示面的图片推定。欧盟 Synjardy 为恩格列净/二甲双胍普通片产品资料，不能与美国 SYNJARDY XR 缓释片合并。",
    "dosageFormClass": "恩格列净/盐酸二甲双胍薄膜衣缓释口服片：5 mg/1,000 mg、10 mg/1,000 mg、12.5 mg/1,000 mg、25 mg/1,000 mg；美国标签要求整片吞服，不得掰开、压碎、溶解或咀嚼",
    "dosageFormClassCode": "oral_modified_release",
    "route": "口服（固定复方缓释片准确产品身份字段）",
    "routeCode": "oral",
    "historicalApprovalEntry": "2015（当前美国公开标签所列 Initial U.S. Approval）",
    "archiveSponsorText": "Boehringer Ingelheim Pharmaceuticals, Inc.（当前美国公开品牌标签所列）"
  },
  "matchPolicy": {
    "contract": "reviewed_name_and_exclusion_cues_v1",
    "exactMatchNames": [],
    "excludedProductCues": [
      "JARDIANCE",
      "empagliflozin tablet",
      "GLUCOPHAGE",
      "metformin tablet",
      "SYNJARDY immediate-release",
      "SYNJARDY tablets",
      "GLYXAMBI",
      "TRIJARDY XR",
      "XIGDUO XR",
      "INVOKAMET XR"
    ],
    "exclusionPrecedence": "before_name_candidate"
  },
  "productPresentations": [
    {
      "id": "us-synjardy-xr-empagliflozin-10mg-metformin-1000mg-0597028073",
      "marketCode": "US",
      "labelVersion": {
        "zh": "DailyMed 当前美国公开标签（SPL v18；2026-08-21 发布）",
        "en": "current U.S. DailyMed public label (SPL v18; published 21 Aug 2026)"
      },
      "dosageForm": {
        "zh": "恩格列净/盐酸二甲双胍薄膜衣缓释片",
        "en": "empagliflozin/metformin hydrochloride film-coated extended-release tablet"
      },
      "route": {
        "zh": "口服；缓释片必须整片吞服",
        "en": "oral; extended-release tablet must be swallowed whole"
      },
      "routeCodes": [
        "oral"
      ],
      "productCode": "NDC 0597-0280-73",
      "pouchCode": null,
      "applicationNumber": null,
      "presentationRole": null,
      "primaryStrengthBasisCode": "per_tablet",
      "primaryDisplay": {
        "zh": "每片恩格列净 10 mg + 盐酸二甲双胍 1,000 mg；30 片瓶装",
        "en": "10 mg empagliflozin + 1,000 mg metformin HCl per tablet; 30-tablet bottle"
      },
      "imageUrl": "https://dailymed.nlm.nih.gov/dailymed/image.cfm?name=synjardy-09.jpg&setid=8006ba29-ee3a-f852-a9bb-c8ec9b41cf66",
      "visualStatus": "exact_public_label_package_image",
      "labeledQuantities": [
        {
          "ingredient": {
            "zh": "恩格列净",
            "en": "empagliflozin"
          },
          "value": 10,
          "unit": "mg",
          "basisCode": "per_tablet",
          "basisLabel": {
            "zh": "每片第一种活性成分标示量；不是个人片数或换算指令",
            "en": "labelled amount of the first active ingredient per tablet; not an individual tablet count or conversion instruction"
          }
        },
        {
          "ingredient": {
            "zh": "盐酸二甲双胍",
            "en": "metformin hydrochloride"
          },
          "value": 1000,
          "unit": "mg",
          "basisCode": "per_tablet",
          "basisLabel": {
            "zh": "每片第二种活性成分标示量；不是个人片数或换算指令",
            "en": "labelled amount of the second active ingredient per tablet; not an individual tablet count or conversion instruction"
          }
        }
      ],
      "concentration": null,
      "container": {
        "typeCode": "bottle",
        "typeLabel": {
          "zh": "塑料瓶",
          "en": "plastic bottle"
        },
        "fill": null,
        "countPerPackage": 30,
        "countUnit": {
          "zh": "片/瓶",
          "en": "tablets per bottle"
        }
      },
      "deliveryDevice": null,
      "compatibleReusableDevice": null,
      "listingStatus": null,
      "package": {
        "count": 30,
        "unit": {
          "zh": "片/瓶",
          "en": "tablets per bottle"
        }
      },
      "physicalClues": {
        "color": {
          "zh": "橙色",
          "en": "orange"
        },
        "shape": {
          "zh": "椭圆形、双凸、无刻痕薄膜衣片",
          "en": "oval, biconvex, unscored film-coated tablet"
        },
        "imprint": "BI symbol / S10 / 1000 M",
        "scoreStatus": "unscored",
        "patchAreaCm2": null
      },
      "comparisonNotice": null,
      "source": {
        "id": "src_527bcad202bf135e",
        "label": "DailyMed（NLM）：SYNJARDY XR 10 mg/1,000 mg、NDC 0597-0280-73、30 片瓶装美国当前标签面板",
        "url": "https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=8006ba29-ee3a-f852-a9bb-c8ec9b41cf66",
        "audience": "public",
        "reviewStatus": "approved",
        "publish": true,
        "documentStatus": "current_regulatory_record",
        "documentKind": "product_label",
        "market": "US",
        "accessStatus": "public_access_confirmed",
        "accessMode": "public_web_page",
        "accessVerifiedAt": "2026-08-30",
        "reviewedAt": "2026-08-30"
      },
      "scope": "package_and_label_identity_only_not_personal_dosing_or_conversion"
    },
    {
      "id": "us-synjardy-xr-empagliflozin-5mg-metformin-1000mg-0597029074",
      "marketCode": "US",
      "labelVersion": {
        "zh": "DailyMed 当前美国公开标签（SPL v18；2026-08-21 发布）",
        "en": "current U.S. DailyMed public label (SPL v18; published 21 Aug 2026)"
      },
      "dosageForm": {
        "zh": "恩格列净/盐酸二甲双胍薄膜衣缓释片",
        "en": "empagliflozin/metformin hydrochloride film-coated extended-release tablet"
      },
      "route": {
        "zh": "口服；缓释片必须整片吞服",
        "en": "oral; extended-release tablet must be swallowed whole"
      },
      "routeCodes": [
        "oral"
      ],
      "productCode": "NDC 0597-0290-74",
      "pouchCode": null,
      "applicationNumber": null,
      "presentationRole": null,
      "primaryStrengthBasisCode": "per_tablet",
      "primaryDisplay": {
        "zh": "每片恩格列净 5 mg + 盐酸二甲双胍 1,000 mg；60 片瓶装",
        "en": "5 mg empagliflozin + 1,000 mg metformin HCl per tablet; 60-tablet bottle"
      },
      "imageUrl": "https://dailymed.nlm.nih.gov/dailymed/image.cfm?name=synjardy-10.jpg&setid=8006ba29-ee3a-f852-a9bb-c8ec9b41cf66",
      "visualStatus": "exact_public_label_package_image",
      "labeledQuantities": [
        {
          "ingredient": {
            "zh": "恩格列净",
            "en": "empagliflozin"
          },
          "value": 5,
          "unit": "mg",
          "basisCode": "per_tablet",
          "basisLabel": {
            "zh": "每片第一种活性成分标示量；不是个人片数或换算指令",
            "en": "labelled amount of the first active ingredient per tablet; not an individual tablet count or conversion instruction"
          }
        },
        {
          "ingredient": {
            "zh": "盐酸二甲双胍",
            "en": "metformin hydrochloride"
          },
          "value": 1000,
          "unit": "mg",
          "basisCode": "per_tablet",
          "basisLabel": {
            "zh": "每片第二种活性成分标示量；不是个人片数或换算指令",
            "en": "labelled amount of the second active ingredient per tablet; not an individual tablet count or conversion instruction"
          }
        }
      ],
      "concentration": null,
      "container": {
        "typeCode": "bottle",
        "typeLabel": {
          "zh": "塑料瓶",
          "en": "plastic bottle"
        },
        "fill": null,
        "countPerPackage": 60,
        "countUnit": {
          "zh": "片/瓶",
          "en": "tablets per bottle"
        }
      },
      "deliveryDevice": null,
      "compatibleReusableDevice": null,
      "listingStatus": null,
      "package": {
        "count": 60,
        "unit": {
          "zh": "片/瓶",
          "en": "tablets per bottle"
        }
      },
      "physicalClues": {
        "color": {
          "zh": "橄榄绿色",
          "en": "olive green"
        },
        "shape": {
          "zh": "椭圆形、双凸、无刻痕薄膜衣片",
          "en": "oval, biconvex, unscored film-coated tablet"
        },
        "imprint": "BI symbol / S5 / 1000 M",
        "scoreStatus": "unscored",
        "patchAreaCm2": null
      },
      "comparisonNotice": null,
      "source": {
        "id": "src_527bcad202bf135e",
        "label": "DailyMed（NLM）：SYNJARDY XR 5 mg/1,000 mg、NDC 0597-0290-74、60 片瓶装美国当前标签面板",
        "url": "https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=8006ba29-ee3a-f852-a9bb-c8ec9b41cf66",
        "audience": "public",
        "reviewStatus": "approved",
        "publish": true,
        "documentStatus": "current_regulatory_record",
        "documentKind": "product_label",
        "market": "US",
        "accessStatus": "public_access_confirmed",
        "accessMode": "public_web_page",
        "accessVerifiedAt": "2026-08-30",
        "reviewedAt": "2026-08-30"
      },
      "scope": "package_and_label_identity_only_not_personal_dosing_or_conversion"
    },
    {
      "id": "us-synjardy-xr-empagliflozin-25mg-metformin-1000mg-0597029588",
      "marketCode": "US",
      "labelVersion": {
        "zh": "DailyMed 当前美国公开标签（SPL v18；2026-08-21 发布）",
        "en": "current U.S. DailyMed public label (SPL v18; published 21 Aug 2026)"
      },
      "dosageForm": {
        "zh": "恩格列净/盐酸二甲双胍薄膜衣缓释片",
        "en": "empagliflozin/metformin hydrochloride film-coated extended-release tablet"
      },
      "route": {
        "zh": "口服；缓释片必须整片吞服",
        "en": "oral; extended-release tablet must be swallowed whole"
      },
      "routeCodes": [
        "oral"
      ],
      "productCode": "NDC 0597-0295-88",
      "pouchCode": null,
      "applicationNumber": null,
      "presentationRole": null,
      "primaryStrengthBasisCode": "per_tablet",
      "primaryDisplay": {
        "zh": "每片恩格列净 25 mg + 盐酸二甲双胍 1,000 mg；30 片瓶装",
        "en": "25 mg empagliflozin + 1,000 mg metformin HCl per tablet; 30-tablet bottle"
      },
      "imageUrl": "https://dailymed.nlm.nih.gov/dailymed/image.cfm?name=synjardy-11.jpg&setid=8006ba29-ee3a-f852-a9bb-c8ec9b41cf66",
      "visualStatus": "exact_public_label_package_image",
      "labeledQuantities": [
        {
          "ingredient": {
            "zh": "恩格列净",
            "en": "empagliflozin"
          },
          "value": 25,
          "unit": "mg",
          "basisCode": "per_tablet",
          "basisLabel": {
            "zh": "每片第一种活性成分标示量；不是个人片数或换算指令",
            "en": "labelled amount of the first active ingredient per tablet; not an individual tablet count or conversion instruction"
          }
        },
        {
          "ingredient": {
            "zh": "盐酸二甲双胍",
            "en": "metformin hydrochloride"
          },
          "value": 1000,
          "unit": "mg",
          "basisCode": "per_tablet",
          "basisLabel": {
            "zh": "每片第二种活性成分标示量；不是个人片数或换算指令",
            "en": "labelled amount of the second active ingredient per tablet; not an individual tablet count or conversion instruction"
          }
        }
      ],
      "concentration": null,
      "container": {
        "typeCode": "bottle",
        "typeLabel": {
          "zh": "塑料瓶",
          "en": "plastic bottle"
        },
        "fill": null,
        "countPerPackage": 30,
        "countUnit": {
          "zh": "片/瓶",
          "en": "tablets per bottle"
        }
      },
      "deliveryDevice": null,
      "compatibleReusableDevice": null,
      "listingStatus": null,
      "package": {
        "count": 30,
        "unit": {
          "zh": "片/瓶",
          "en": "tablets per bottle"
        }
      },
      "physicalClues": {
        "color": {
          "zh": "浅绿色",
          "en": "light green"
        },
        "shape": {
          "zh": "椭圆形、双凸、无刻痕薄膜衣片",
          "en": "oval, biconvex, unscored film-coated tablet"
        },
        "imprint": "BI symbol / S25 / 1000 M",
        "scoreStatus": "unscored",
        "patchAreaCm2": null
      },
      "comparisonNotice": null,
      "source": {
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        "label": "DailyMed（NLM）：SYNJARDY XR 25 mg/1,000 mg、NDC 0597-0295-88、30 片瓶装美国当前标签面板",
        "url": "https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=8006ba29-ee3a-f852-a9bb-c8ec9b41cf66",
        "audience": "public",
        "reviewStatus": "approved",
        "publish": true,
        "documentStatus": "current_regulatory_record",
        "documentKind": "product_label",
        "market": "US",
        "accessStatus": "public_access_confirmed",
        "accessMode": "public_web_page",
        "accessVerifiedAt": "2026-08-30",
        "reviewedAt": "2026-08-30"
      },
      "scope": "package_and_label_identity_only_not_personal_dosing_or_conversion"
    },
    {
      "id": "us-synjardy-xr-empagliflozin-12-5mg-metformin-1000mg-0597030045",
      "marketCode": "US",
      "labelVersion": {
        "zh": "DailyMed 当前美国公开标签（SPL v18；2026-08-21 发布）",
        "en": "current U.S. DailyMed public label (SPL v18; published 21 Aug 2026)"
      },
      "dosageForm": {
        "zh": "恩格列净/盐酸二甲双胍薄膜衣缓释片",
        "en": "empagliflozin/metformin hydrochloride film-coated extended-release tablet"
      },
      "route": {
        "zh": "口服；缓释片必须整片吞服",
        "en": "oral; extended-release tablet must be swallowed whole"
      },
      "routeCodes": [
        "oral"
      ],
      "productCode": "NDC 0597-0300-45",
      "pouchCode": null,
      "applicationNumber": null,
      "presentationRole": null,
      "primaryStrengthBasisCode": "per_tablet",
      "primaryDisplay": {
        "zh": "每片恩格列净 12.5 mg + 盐酸二甲双胍 1,000 mg；60 片瓶装",
        "en": "12.5 mg empagliflozin + 1,000 mg metformin HCl per tablet; 60-tablet bottle"
      },
      "imageUrl": "https://dailymed.nlm.nih.gov/dailymed/image.cfm?name=synjardy-12.jpg&setid=8006ba29-ee3a-f852-a9bb-c8ec9b41cf66",
      "visualStatus": "exact_public_label_package_image",
      "labeledQuantities": [
        {
          "ingredient": {
            "zh": "恩格列净",
            "en": "empagliflozin"
          },
          "value": 12.5,
          "unit": "mg",
          "basisCode": "per_tablet",
          "basisLabel": {
            "zh": "每片第一种活性成分标示量；不是个人片数或换算指令",
            "en": "labelled amount of the first active ingredient per tablet; not an individual tablet count or conversion instruction"
          }
        },
        {
          "ingredient": {
            "zh": "盐酸二甲双胍",
            "en": "metformin hydrochloride"
          },
          "value": 1000,
          "unit": "mg",
          "basisCode": "per_tablet",
          "basisLabel": {
            "zh": "每片第二种活性成分标示量；不是个人片数或换算指令",
            "en": "labelled amount of the second active ingredient per tablet; not an individual tablet count or conversion instruction"
          }
        }
      ],
      "concentration": null,
      "container": {
        "typeCode": "bottle",
        "typeLabel": {
          "zh": "塑料瓶",
          "en": "plastic bottle"
        },
        "fill": null,
        "countPerPackage": 60,
        "countUnit": {
          "zh": "片/瓶",
          "en": "tablets per bottle"
        }
      },
      "deliveryDevice": null,
      "compatibleReusableDevice": null,
      "listingStatus": null,
      "package": {
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        "unit": {
          "zh": "片/瓶",
          "en": "tablets per bottle"
        }
      },
      "physicalClues": {
        "color": {
          "zh": "蓝色",
          "en": "blue"
        },
        "shape": {
          "zh": "椭圆形、双凸、无刻痕薄膜衣片",
          "en": "oval, biconvex, unscored film-coated tablet"
        },
        "imprint": "BI symbol / S12 / 1000 M",
        "scoreStatus": "unscored",
        "patchAreaCm2": null
      },
      "comparisonNotice": null,
      "source": {
        "id": "src_527bcad202bf135e",
        "label": "DailyMed（NLM）：SYNJARDY XR 12.5 mg/1,000 mg、NDC 0597-0300-45、60 片瓶装美国当前标签面板",
        "url": "https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=8006ba29-ee3a-f852-a9bb-c8ec9b41cf66",
        "audience": "public",
        "reviewStatus": "approved",
        "publish": true,
        "documentStatus": "current_regulatory_record",
        "documentKind": "product_label",
        "market": "US",
        "accessStatus": "public_access_confirmed",
        "accessMode": "public_web_page",
        "accessVerifiedAt": "2026-08-30",
        "reviewedAt": "2026-08-30"
      },
      "scope": "package_and_label_identity_only_not_personal_dosing_or_conversion"
    }
  ],
  "comparisonPresentations": [],
  "appearanceReferences": [],
  "visualReference": {
    "presentationId": "us-synjardy-xr-empagliflozin-10mg-metformin-1000mg-0597028073",
    "status": "historical_public_label_image_not_product_authentication",
    "imageUrl": "https://dailymed.nlm.nih.gov/dailymed/image.cfm?name=synjardy-09.jpg&setid=8006ba29-ee3a-f852-a9bb-c8ec9b41cf66",
    "alt": "SYNJARDY XR 恩格列净 10 mg/盐酸二甲双胍 1,000 mg、NDC 0597-0280-73、30 片瓶装的美国 DailyMed 当前标签展示面",
    "archiveMarket": "美国",
    "labelVersion": "DailyMed SPL v18；2026-08-21 发布",
    "presentation": "SYNJARDY XR 每片恩格列净 10 mg/盐酸二甲双胍 1,000 mg，NDC 0597-0280-73，30 片瓶装标签展示面。",
    "notice": "此图只对应所引美国标签中的 10 mg/1,000 mg、NDC 0597-0280-73、30 片瓶装；不代表另三张展示面、同强度其他瓶装 NDC、SYNJARDY 普通片、其他市场包装或当前可得性，不用于鉴定真伪，也不生成个人片数。",
    "source": {
      "id": "src_527bcad202bf135e",
      "label": "DailyMed（NLM）：SYNJARDY XR 10 mg/1,000 mg、NDC 0597-0280-73、30 片瓶装美国当前标签面板",
      "url": "https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=8006ba29-ee3a-f852-a9bb-c8ec9b41cf66",
      "audience": "public",
      "reviewStatus": "approved",
      "publish": true,
      "documentStatus": "current_regulatory_record",
      "documentKind": "product_label",
      "market": "US",
      "accessStatus": "public_access_confirmed",
      "accessMode": "public_web_page",
      "accessVerifiedAt": "2026-08-30",
      "reviewedAt": "2026-08-30"
    }
  },
  "visualCoverageNote": null,
  "labelReading": {
    "coverage": "drug_specific_source_review",
    "title": {
      "zh": "SYNJARDY XR 说明书放大阅读：一片两种成分，缓释片不得掰开、压碎、溶解或咀嚼",
      "en": "SYNJARDY XR label reading: two ingredients in one tablet; do not split, crush, dissolve or chew the extended-release tablet"
    },
    "summary": {
      "zh": "当前美国标签列四种强度，每片二甲双胍部分均为 1,000 mg，恩格列净分别为 5、10、12.5 或 25 mg。先确认准确 NDC 和两个成分数字，不要相加、按外观估算后掰片，或再自行加用 JARDIANCE、恩格列净、GLUCOPHAGE 或二甲双胍产品。",
      "en": "The current U.S. label lists four strengths. Every tablet contains 1,000 mg metformin HCl, while empagliflozin is 5, 10, 12.5 or 25 mg. Confirm the exact NDC and both ingredient figures; do not add the numbers, estimate and split from appearance, or self-add JARDIANCE/empagliflozin, GLUCOPHAGE or metformin products."
    },
    "checks": [
      {
        "zh": "例如“10 mg/1,000 mg”表示每片含恩格列净 10 mg 和盐酸二甲双胍 1,000 mg；它不是 1,010 mg 的可比强度，也不是早晚两个时间。",
        "en": "For example, 10 mg/1,000 mg means 10 mg empagliflozin and 1,000 mg metformin HCl per tablet. It is not a comparable 1,010 mg strength or two times of day."
      },
      {
        "zh": "标签要求早晨随餐整片吞服，并明确不得掰开、压碎、溶解或咀嚼。网页只解释标签文字，不根据这一句替任何人选择时间、频次、片数或替代剂型。",
        "en": "The label says to swallow whole with a meal in the morning and not to split, crush, dissolve or chew. The site explains that text only; it does not select an individual's time, frequency, tablet count or alternative dosage form."
      },
      {
        "zh": "黑框警示涉及二甲双胍相关乳酸性酸中毒，标签还涉及酮症酸中毒、脱水/低血压、肾功能、泌尿生殖感染、手术与含碘造影。65 岁及以上、多病或多药使用者尤其应带完整药单核对。",
        "en": "The boxed warning covers metformin-associated lactic acidosis, while the label also covers ketoacidosis, volume depletion/hypotension, kidney function, genitourinary infection, surgery and iodinated contrast. People aged 65 or older and those with several conditions or medicines should especially bring the complete medicine list for review."
      },
      {
        "zh": "呼吸困难、严重虚弱、持续呕吐、明显意识变化、严重腹痛或其他急性重症需要立即使用当地急救渠道并带上全部药盒；不要等待网页判断是否停药或补服。",
        "en": "Breathing difficulty, severe weakness, persistent vomiting, marked altered awareness, severe abdominal pain or another acute serious concern requires local emergency help with every medicine pack. Do not wait for a webpage to decide interruption or make-up use."
      }
    ],
    "source": {
      "id": "src_527bcad202bf135e",
      "label": "DailyMed（NLM）：SYNJARDY XR 当前美国公开标签与 Medication Guide（2026-08 更新）",
      "url": "https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=8006ba29-ee3a-f852-a9bb-c8ec9b41cf66",
      "audience": "public",
      "reviewStatus": "approved",
      "publish": true,
      "documentStatus": "current_regulatory_record",
      "documentKind": "product_label",
      "market": "US",
      "accessStatus": "public_access_confirmed",
      "accessMode": "public_web_page",
      "accessVerifiedAt": "2026-08-30",
      "reviewedAt": "2026-08-30"
    },
    "scope": "label_literacy_only_no_individual_dosing_or_substitution"
  },
  "mechanismReading": {
    "title": {
      "zh": "两种成分怎样配合：恩格列净影响肾脏葡萄糖重吸收，二甲双胍影响肝糖生成与胰岛素敏感性",
      "en": "How the ingredients work: empagliflozin affects renal glucose reabsorption, while metformin affects hepatic glucose production and insulin sensitivity"
    },
    "summary": {
      "zh": "标签把恩格列净列为 SGLT2 抑制剂，把二甲双胍列为双胍类。两条作用路径解释固定复方的组成，但不能推导个人该选哪种强度、是否适合、何时停用或是否应与其他降糖药联合。",
      "en": "The label identifies empagliflozin as an SGLT2 inhibitor and metformin as a biguanide. The two pathways explain the fixed combination but cannot determine an individual's strength, suitability, interruption or combination with another glucose-lowering medicine."
    },
    "checks": [
      {
        "zh": "“两种机制互补”不是把 JARDIANCE 和二甲双胍自行拼成 SYNJARDY XR 的许可；缓释核心、即时释放包衣、成分量、标签和监测边界属于准确产品。",
        "en": "“Complementary mechanisms” do not permit self-assembling SYNJARDY XR from JARDIANCE and metformin. The extended-release core, immediate-release coating, ingredient amounts, label and monitoring boundaries belong to the exact product."
      },
      {
        "zh": "标签说明该片由盐酸二甲双胍缓释核心和含即时释放恩格列净的外层组成；这正是不能仅按毫克数或外观看成普通片、拆分片或两盒单方的原因。",
        "en": "The label states that the tablet has a metformin HCl extended-release core coated with immediate-release empagliflozin. That is why milligram figures or appearance cannot turn it into an immediate-release tablet, a divided tablet or two single-ingredient packs."
      },
      {
        "zh": "基因筛查不是网页替个人选择这款药的默认答案。个体适用性要结合诊断、肾肝功能、完整药单、既往反应和目标市场现行说明书，由负责团队判断。",
        "en": "Genetic screening is not the site's default answer for choosing this medicine. Individual suitability requires diagnosis, renal and hepatic function, the complete medicine list, prior response and the current target-market label, reviewed by the treating team."
      }
    ],
    "source": {
      "id": "src_527bcad202bf135e",
      "label": "DailyMed（NLM）：SYNJARDY XR 当前美国公开标签（12.1 Mechanism of Action 与产品结构）",
      "url": "https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=8006ba29-ee3a-f852-a9bb-c8ec9b41cf66",
      "audience": "public",
      "reviewStatus": "approved",
      "publish": true,
      "documentStatus": "current_regulatory_record",
      "documentKind": "product_label",
      "market": "US",
      "accessStatus": "public_access_confirmed",
      "accessMode": "public_web_page",
      "accessVerifiedAt": "2026-08-30",
      "reviewedAt": "2026-08-30"
    },
    "scope": "mechanism_literacy_only_no_individual_dosing_or_substitution"
  },
  "pharmacovigilance": {
    "status": "official_routes_only_no_live_alert_inference",
    "reviewedAt": "2026-08-22",
    "identity": {
      "brand": "SYNJARDY XR",
      "generic": "恩格列净/盐酸二甲双胍缓释片",
      "dosageFormClass": "恩格列净/盐酸二甲双胍薄膜衣缓释口服片：5 mg/1,000 mg、10 mg/1,000 mg、12.5 mg/1,000 mg、25 mg/1,000 mg；美国标签要求整片吞服，不得掰开、压碎、溶解或咀嚼"
    },
    "labelSource": {
      "id": "src_527bcad202bf135e",
      "label": "DailyMed（NLM）：SYNJARDY XR 当前美国公开品牌标签、四种展示包装与 Medication Guide（SPL v18；2026-08-21 发布）",
      "url": "https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=8006ba29-ee3a-f852-a9bb-c8ec9b41cf66",
      "audience": "public",
      "reviewStatus": "approved",
      "publish": true,
      "documentStatus": "current_regulatory_record",
      "documentKind": "product_label",
      "market": "US",
      "accessStatus": "public_access_confirmed",
      "accessMode": "public_web_page",
      "accessVerifiedAt": "2026-08-30",
      "reviewedAt": "2026-08-30"
    },
    "productRoutes": [
      {
        "source": {
          "id": "src_527bcad202bf135e",
          "label": "DailyMed（NLM）：SYNJARDY XR 当前美国公开品牌标签、四种展示包装与 Medication Guide（SPL v18；2026-08-21 发布）",
          "url": "https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=8006ba29-ee3a-f852-a9bb-c8ec9b41cf66",
          "audience": "public",
          "reviewStatus": "approved",
          "publish": true,
          "documentStatus": "current_regulatory_record",
          "documentKind": "product_label",
          "market": "US",
          "accessStatus": "public_access_confirmed",
          "accessMode": "public_web_page",
          "accessVerifiedAt": "2026-08-30",
          "reviewedAt": "2026-08-30"
        },
        "status": "product_level_public_record_verified",
        "authority": {
          "zh": "美国国家医学图书馆 DailyMed",
          "en": "U.S. National Library of Medicine DailyMed"
        },
        "market": {
          "zh": "美国",
          "en": "United States"
        },
        "recordType": {
          "zh": "公开药品标签",
          "en": "Public medicine label"
        },
        "reviewedAt": "2026-08-30",
        "scope": {
          "zh": "已逐项核对本档案可公开访问的产品级来源入口。该核对不代表已完成所有国家或地区的实时警示检索，也不代表该药存在或不存在当前风险。",
          "en": "This dossier’s publicly accessible product-level route has been checked individually. It does not mean that real-time alerts in every country or region have been searched, or that the medicine has or does not have a current risk."
        }
      }
    ],
    "recordRoute": {
      "status": "product_level_public_record_verified",
      "authority": {
        "zh": "美国国家医学图书馆 DailyMed",
        "en": "U.S. National Library of Medicine DailyMed"
      },
      "market": {
        "zh": "美国",
        "en": "United States"
      },
      "recordType": {
        "zh": "公开药品标签",
        "en": "Public medicine label"
      },
      "reviewedAt": "2026-08-30",
      "scope": {
        "zh": "已逐项核对本档案可公开访问的产品级来源入口。该核对不代表已完成所有国家或地区的实时警示检索，也不代表该药存在或不存在当前风险。",
        "en": "This dossier’s publicly accessible product-level route has been checked individually. It does not mean that real-time alerts in every country or region have been searched, or that the medicine has or does not have a current risk."
      }
    },
    "channels": [
      {
        "id": "china-nmpa-drug-evaluation-centre",
        "authority": "NMPA 药品评价中心",
        "market": {
          "zh": "中国大陆",
          "en": "Mainland China"
        },
        "title": {
          "zh": "药物警戒快讯与安全警示",
          "en": "Drug-vigilance bulletins and safety notices"
        },
        "purpose": {
          "zh": "国家药监局药品评价中心发布的药物警戒快讯、安全警示及药品不良反应监测相关原始入口；具体产品仍须按批准文号、剂型、规格、持有人和公告日期逐项核对。",
          "en": "Primary NMPA Drug Evaluation Centre gateway for drug-vigilance bulletins, safety notices and adverse-reaction monitoring. Exact products still require checking approval number, dosage form, strength, authorisation holder and notice date item by item."
        },
        "source": {
          "id": "src_05ff2860226564d4",
          "label": "国家药监局药品评价中心：药物警戒与安全警示入口",
          "url": "https://www.cdr-adr.org.cn/",
          "audience": "public",
          "reviewStatus": "approved",
          "publish": true,
          "documentStatus": "official_safety_monitoring",
          "documentKind": "regulatory_safety_communication",
          "market": "CN",
          "accessStatus": "public_access_confirmed",
          "accessMode": "public_web_page",
          "accessVerifiedAt": "2026-08-22",
          "reviewedAt": "2026-08-22"
        }
      },
      {
        "id": "fda-drug-safety-communications",
        "authority": "FDA",
        "market": {
          "zh": "美国",
          "en": "United States"
        },
        "title": {
          "zh": "药物安全通讯",
          "en": "Drug Safety Communications"
        },
        "purpose": {
          "zh": "监管机构就重要新安全问题、标签变化或风险沟通发布的原始页面。",
          "en": "Primary FDA pages for important new safety issues, labelling changes and risk communications."
        },
        "source": {
          "id": "src_9177df9e1825aa72",
          "label": "FDA：Drug Safety Communications",
          "url": "https://www.fda.gov/drugs/drug-safety-and-availability/drug-safety-communications",
          "audience": "public",
          "reviewStatus": "approved",
          "publish": true,
          "documentStatus": "official_safety_monitoring",
          "documentKind": "regulatory_safety_communication",
          "market": "US",
          "accessStatus": "public_access_confirmed",
          "accessMode": "public_web_page",
          "accessVerifiedAt": "2026-08-22",
          "reviewedAt": "2026-08-22"
        }
      },
      {
        "id": "fda-medwatch",
        "authority": "FDA MedWatch",
        "market": {
          "zh": "美国",
          "en": "United States"
        },
        "title": {
          "zh": "安全信息与严重问题报告",
          "en": "Safety information and serious-problem reporting"
        },
        "purpose": {
          "zh": "美国 MedWatch 的安全信息和报告入口；报告不等同于已证实因果关系。",
          "en": "U.S. MedWatch safety-information and reporting gateway; a report does not itself establish causality."
        },
        "source": {
          "id": "src_e4739cd55d27ab51",
          "label": "FDA：MedWatch 药品安全信息与不良事件报告计划",
          "url": "https://www.fda.gov/safety/medwatch-fda-safety-information-and-adverse-event-reporting-program",
          "audience": "public",
          "reviewStatus": "approved",
          "publish": true,
          "documentStatus": "official_safety_monitoring",
          "documentKind": "adverse_event_reporting",
          "market": "US",
          "accessStatus": "public_access_confirmed",
          "accessMode": "public_web_page",
          "accessVerifiedAt": "2026-08-22",
          "reviewedAt": "2026-08-22"
        }
      },
      {
        "id": "ema-pharmacovigilance",
        "authority": "EMA",
        "market": {
          "zh": "欧盟/欧洲经济区",
          "en": "European Union / European Economic Area"
        },
        "title": {
          "zh": "药物警戒概览与 EudraVigilance",
          "en": "Pharmacovigilance overview and EudraVigilance"
        },
        "purpose": {
          "zh": "欧盟药物警戒、疑似不良反应报告和 PRAC 安全评估的官方入口。",
          "en": "Official EU gateway for pharmacovigilance, suspected adverse-reaction reports and PRAC safety assessment."
        },
        "source": {
          "id": "src_2ad42a3deae747d1",
          "label": "EMA：Pharmacovigilance overview",
          "url": "https://www.ema.europa.eu/en/human-regulatory-overview/pharmacovigilance-overview",
          "audience": "public",
          "reviewStatus": "approved",
          "publish": true,
          "documentStatus": "official_safety_monitoring",
          "documentKind": "regulatory_safety_communication",
          "market": "EU",
          "accessStatus": "public_access_confirmed",
          "accessMode": "javascript_or_cookie_controls",
          "accessVerifiedAt": "2026-08-22",
          "reviewedAt": "2026-08-22"
        }
      },
      {
        "id": "mhra-drug-safety-update",
        "authority": "MHRA",
        "market": {
          "zh": "英国",
          "en": "United Kingdom"
        },
        "title": {
          "zh": "Drug Safety Update",
          "en": "Drug Safety Update"
        },
        "purpose": {
          "zh": "英国 MHRA 面向专业人士和公众的药品安全更新原始发布页。",
          "en": "Primary UK MHRA medicine-safety updates for professionals and the public."
        },
        "source": {
          "id": "src_23fdbe67abeafc63",
          "label": "MHRA：Drug Safety Update",
          "url": "https://www.gov.uk/drug-safety-update",
          "audience": "public",
          "reviewStatus": "approved",
          "publish": true,
          "documentStatus": "official_safety_monitoring",
          "documentKind": "regulatory_safety_communication",
          "market": "UK",
          "accessStatus": "public_access_confirmed",
          "accessMode": "public_web_page",
          "accessVerifiedAt": "2026-08-22",
          "reviewedAt": "2026-08-22"
        }
      },
      {
        "id": "pmda-drug-safety",
        "authority": "PMDA",
        "market": {
          "zh": "日本",
          "en": "Japan"
        },
        "title": {
          "zh": "药品安全信息",
          "en": "Medicine safety information"
        },
        "purpose": {
          "zh": "日本 PMDA 药品安全信息的英文官方入口；具体产品仍应以日文产品页和现行文件复核。",
          "en": "PMDA’s English official safety gateway; exact products still require checking against the Japanese product page and current documents."
        },
        "source": {
          "id": "src_06d6be2880f12024",
          "label": "PMDA：Safety Information Regarding Drugs",
          "url": "https://www.pmda.go.jp/english/safety/info-services/drugs/0001.html",
          "audience": "public",
          "reviewStatus": "approved",
          "publish": true,
          "documentStatus": "official_safety_monitoring",
          "documentKind": "regulatory_safety_communication",
          "market": "JP",
          "accessStatus": "public_access_confirmed",
          "accessMode": "public_web_page",
          "accessVerifiedAt": "2026-08-22",
          "reviewedAt": "2026-08-22"
        }
      },
      {
        "id": "mfds-drug-safety-letters",
        "authority": "MFDS",
        "market": {
          "zh": "韩国",
          "en": "Republic of Korea"
        },
        "title": {
          "zh": "药品安全性书信",
          "en": "Medicine safety letters"
        },
        "purpose": {
          "zh": "韩国 MFDS 发布的药品安全性书信原始索引。原文为韩文，须按涉及产品、剂型、市场和日期逐项阅读；它不自动适用于其他市场，也不构成对个人情况的结论。",
          "en": "MFDS’s primary index for medicine safety letters in the Republic of Korea. The original notices are in Korean and must be read against the named product, dosage form, market and date; they do not automatically apply in another market or decide an individual case."
        },
        "source": {
          "id": "src_2d7f5018cd05eff4",
          "label": "MFDS：药品安全性书信（韩文原始资料）",
          "url": "https://www.mfds.go.kr/brd/m_545/list.do",
          "audience": "public",
          "reviewStatus": "approved",
          "publish": true,
          "documentStatus": "official_safety_monitoring",
          "documentKind": "regulatory_safety_communication",
          "market": "KR",
          "accessStatus": "public_access_confirmed",
          "accessMode": "public_web_page",
          "accessVerifiedAt": "2026-08-22",
          "reviewedAt": "2026-08-22"
        }
      },
      {
        "id": "hsa-adverse-events",
        "authority": "HSA",
        "market": {
          "zh": "新加坡",
          "en": "Singapore"
        },
        "title": {
          "zh": "不良反应报告与药物安全信息",
          "en": "Adverse-event reporting and medicine-safety information"
        },
        "purpose": {
          "zh": "新加坡 HSA 面向公众的疑似不良反应报告、药物安全信息与本地监管入口；一份报告不等同于个体因果关系，具体产品仍须按新加坡注册状态、剂型、规格、日期和现行产品资料逐项核对。",
          "en": "HSA’s public Singapore gateway for suspected adverse-event reporting and medicine-safety information. A report does not itself establish individual causality; exact products still require checking Singapore registration status, dosage form, strength, date and current product information."
        },
        "source": {
          "id": "src_9240397d5a8574c1",
          "label": "HSA：Report adverse events",
          "url": "https://www.hsa.gov.sg/adverse-events/",
          "audience": "public",
          "reviewStatus": "approved",
          "publish": true,
          "documentStatus": "official_safety_monitoring",
          "documentKind": "adverse_event_reporting",
          "market": "SG",
          "accessStatus": "public_access_confirmed",
          "accessMode": "public_web_page",
          "accessVerifiedAt": "2026-08-22",
          "reviewedAt": "2026-08-22"
        }
      },
      {
        "id": "health-canada-medeffect-advisories",
        "authority": "Health Canada",
        "market": {
          "zh": "加拿大",
          "en": "Canada"
        },
        "title": {
          "zh": "MedEffect 加拿大：建议、警告与召回",
          "en": "MedEffect Canada: advisories, warnings and recalls"
        },
        "purpose": {
          "zh": "加拿大政府 Health Canada 的 MedEffect 公开入口，汇集药品及健康产品的建议、警告、召回、报告与安全信息；具体产品仍须按市场、剂型、规格、公告日期和批号逐项核对。",
          "en": "Health Canada’s public MedEffect gateway for medicine and health-product advisories, warnings, recalls, reporting and safety information. Exact products still require checking market, dosage form, strength, notice date and lot item by item."
        },
        "source": {
          "id": "src_212ec921fa6634ad",
          "label": "Health Canada：MedEffect Canada 建议、警告与召回",
          "url": "https://www.canada.ca/en/health-canada/services/drugs-health-products/medeffect-canada/advisories-warnings-recalls.html",
          "audience": "public",
          "reviewStatus": "approved",
          "publish": true,
          "documentStatus": "official_safety_monitoring",
          "documentKind": "regulatory_safety_communication",
          "market": "CA",
          "accessStatus": "public_access_confirmed",
          "accessMode": "public_web_page",
          "accessVerifiedAt": "2026-08-22",
          "reviewedAt": "2026-08-22"
        }
      },
      {
        "id": "tga-safety-alerts",
        "authority": "TGA",
        "market": {
          "zh": "澳大利亚",
          "en": "Australia"
        },
        "title": {
          "zh": "药品安全警示",
          "en": "Medicine safety alerts"
        },
        "purpose": {
          "zh": "澳大利亚 TGA 的药品安全警示、建议和监测信息原始发布页。",
          "en": "Primary Australian TGA safety alerts, advisories and monitoring information for therapeutic products."
        },
        "source": {
          "id": "src_ffe6142814f88fac",
          "label": "TGA：Safety alerts",
          "url": "https://www.tga.gov.au/safety/safety-monitoring-and-information/safety-alerts",
          "audience": "public",
          "reviewStatus": "approved",
          "publish": true,
          "documentStatus": "official_safety_monitoring",
          "documentKind": "regulatory_safety_communication",
          "market": "AU",
          "accessStatus": "public_access_confirmed",
          "accessMode": "public_web_page",
          "accessVerifiedAt": "2026-08-22",
          "reviewedAt": "2026-08-22"
        }
      },
      {
        "id": "swissmedic-pharmacovigilance",
        "authority": "Swissmedic",
        "market": {
          "zh": "瑞士",
          "en": "Switzerland"
        },
        "title": {
          "zh": "药物警戒与不良反应报告",
          "en": "Pharmacovigilance and suspected adverse-reaction reporting"
        },
        "purpose": {
          "zh": "瑞士 Swissmedic 的药物警戒、信号评估和疑似不良反应官方入口；报告或信号本身不等同于对个体因果关系的确认。",
          "en": "Official Swissmedic gateway for pharmacovigilance, signal assessment and suspected adverse-reaction reporting; a report or signal does not itself confirm individual causality."
        },
        "source": {
          "id": "src_c854f813ce2671df",
          "label": "Swissmedic：Pharmacovigilance",
          "url": "https://www.swissmedic.ch/swissmedic/en/home/humanarzneimittel/market-surveillance/pharmacovigilance.html",
          "audience": "public",
          "reviewStatus": "approved",
          "publish": true,
          "documentStatus": "official_safety_monitoring",
          "documentKind": "adverse_event_reporting",
          "market": "CH",
          "accessStatus": "public_access_confirmed",
          "accessMode": "public_web_page",
          "accessVerifiedAt": "2026-08-22",
          "reviewedAt": "2026-08-22"
        }
      },
      {
        "id": "medsafe-safety-communications",
        "authority": "Medsafe",
        "market": {
          "zh": "新西兰",
          "en": "New Zealand"
        },
        "title": {
          "zh": "药品安全通讯",
          "en": "Medicine safety communications"
        },
        "purpose": {
          "zh": "新西兰 Medsafe 面向公众和专业人士的药品安全通讯与归档入口；旧公告可能已被现行产品资料更新。",
          "en": "New Zealand Medsafe gateway for public and professional medicine safety communications and archives; older notices may have been superseded by current product information."
        },
        "source": {
          "id": "src_3510c1a523ec9769",
          "label": "Medsafe：Safety Communications",
          "url": "https://www.medsafe.govt.nz/safety/SafetyCommunications.asp",
          "audience": "public",
          "reviewStatus": "approved",
          "publish": true,
          "documentStatus": "official_safety_monitoring",
          "documentKind": "regulatory_safety_communication",
          "market": "NZ",
          "accessStatus": "public_access_confirmed",
          "accessMode": "public_web_page",
          "accessVerifiedAt": "2026-08-22",
          "reviewedAt": "2026-08-22"
        }
      },
      {
        "id": "sahpra-safety-information",
        "authority": "SAHPRA",
        "market": {
          "zh": "南非",
          "en": "South Africa"
        },
        "title": {
          "zh": "药物安全信息、警示与药物警戒",
          "en": "Medicine safety information, alerts and pharmacovigilance"
        },
        "purpose": {
          "zh": "南非 SAHPRA 面向公众和专业人士的药物安全信息、警示与药物警戒入口；官方警示不等同于产品在所有情形下不安全，具体产品仍须按南非注册状态、剂型、规格、公告日期与现行资料逐项核对。",
          "en": "SAHPRA’s safety-information, alerts and pharmacovigilance gateway for the public and professionals in South Africa. An official alert does not itself mean a product is unsafe in every circumstance; exact products still require checking South African registration status, dosage form, strength, notice date and current product information."
        },
        "source": {
          "id": "src_25b0aaefee742163",
          "label": "SAHPRA：Safety Information Updates / Pharmacovigilance",
          "url": "https://www.sahpra.org.za/safety-information-and-updates/",
          "audience": "public",
          "reviewStatus": "approved",
          "publish": true,
          "documentStatus": "official_safety_monitoring",
          "documentKind": "regulatory_safety_communication",
          "market": "ZA",
          "accessStatus": "public_access_confirmed",
          "accessMode": "public_web_page",
          "accessVerifiedAt": "2026-08-22",
          "reviewedAt": "2026-08-22"
        }
      },
      {
        "id": "who-medicine-safety-alerts",
        "authority": "WHO",
        "market": {
          "zh": "全球",
          "en": "Global"
        },
        "title": {
          "zh": "药品与疫苗安全警示档案",
          "en": "Medicine and vaccine safety-alert archive"
        },
        "purpose": {
          "zh": "WHO 的跨市场安全警示档案；每条历史警示必须按公告日期、涉及产品和市场单独阅读。",
          "en": "WHO’s cross-market safety-alert archive; every historical notice must be read against its date, named product and market."
        },
        "source": {
          "id": "src_9a7dc56ec34c7e1a",
          "label": "WHO：Safety alerts for medicines and vaccines",
          "url": "https://www.who.int/teams/regulation-prequalification/regulation-and-safety/pharmacovigilance/safety-alerts",
          "audience": "public",
          "reviewStatus": "approved",
          "publish": true,
          "documentStatus": "official_safety_monitoring",
          "documentKind": "regulatory_safety_communication",
          "market": "GLOBAL",
          "accessStatus": "public_access_confirmed",
          "accessMode": "public_web_page",
          "accessVerifiedAt": "2026-08-22",
          "reviewedAt": "2026-08-22"
        }
      },
      {
        "id": "anvisa-pharmacovigilance",
        "authority": "Anvisa",
        "market": {
          "zh": "巴西",
          "en": "Brazil"
        },
        "title": {
          "zh": "药物警戒、警示与 VigiMed",
          "en": "Pharmacovigilance, alerts and VigiMed"
        },
        "purpose": {
          "zh": "巴西 Anvisa 的药物警戒原始入口，涵盖警示、药物警戒公告、风险沟通和 VigiMed 报告路径；具体产品仍须按巴西批准状态、剂型、规格和公告日期逐项核对。",
          "en": "Anvisa’s primary Brazilian pharmacovigilance gateway for alerts, bulletins, risk communication and VigiMed reporting. Exact products still require checking Brazilian authorisation status, dosage form, strength and notice date item by item."
        },
        "source": {
          "id": "src_5de362c12580111d",
          "label": "Anvisa：Farmacovigilância（药物警戒、警示与 VigiMed）",
          "url": "https://www.gov.br/anvisa/pt-br/assuntos/fiscalizacao-e-monitoramento/farmacovigilancia",
          "audience": "public",
          "reviewStatus": "approved",
          "publish": true,
          "documentStatus": "official_safety_monitoring",
          "documentKind": "regulatory_safety_communication",
          "market": "BR",
          "accessStatus": "public_access_confirmed",
          "accessMode": "public_web_page",
          "accessVerifiedAt": "2026-08-22",
          "reviewedAt": "2026-08-22"
        }
      }
    ],
    "notices": [],
    "boundary": {
      "zh": "本卡将逐药产品级来源与 15 个市场级官方警戒入口放在同一处核验；它不表示已完成该药在所有国家或地区的实时警示检索，也不表示该药存在新的安全警示、召回或风险结论。请先以品牌名、通用名、剂型、规格、所在市场和公告日期逐项匹配；不要仅因看到标题自行停药、换药、加量或减量。",
      "en": "This card brings together the medicine-specific product route and 15 market-level official vigilance gateways. It does not mean real-time alerts for this medicine have been searched in every country or region, or that the medicine has a new alert, recall or risk conclusion. Match brand, generic name, dosage form, strength, market and notice date item by item; do not self-stop, switch, increase or reduce use from a headline."
    },
    "scope": "official_routes_only_no_live_alert_inference"
  },
  "archive": {
    "summary": "SYNJARDY XR 一片同时含恩格列净和盐酸二甲双胍缓释成分。包装上的两个 mg 数字分别属于两种成分，不是相加后的单一强度，也不能与 JARDIANCE、GLUCOPHAGE、SYNJARDY 普通片、XIGDUO XR 或其他复方自行拼接。当前美国标签列四种强度，并要求缓释片整片吞服，不得掰开、压碎、溶解或咀嚼。网页帮助认清准确产品、成分、每片标示量和官方说明书，不生成个人片数、联用、换药、补服或停药方案。",
    "history": "FDA/NLM 当前标签记录 SYNJARDY XR 的美国初始批准年份为 2015，NDA 208658 的营销记录自 2016-12-10 开始；当前 SPL v18 于 2026-08-21 发布。美国 SYNJARDY XR 缓释片和欧盟 Synjardy 普通片属于不同市场、释放形式与文件，不能只凭共同成分或品牌词根合并。",
    "sourceDocuments": [
      {
        "id": "src_527bcad202bf135e",
        "label": "DailyMed（NLM）：SYNJARDY XR 当前美国公开品牌标签、四种展示包装与 Medication Guide（SPL v18；2026-08-21 发布）",
        "url": "https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=8006ba29-ee3a-f852-a9bb-c8ec9b41cf66",
        "audience": "public",
        "reviewStatus": "approved",
        "publish": true,
        "documentStatus": "current_regulatory_record",
        "documentKind": "product_label",
        "market": "US",
        "accessStatus": "public_access_confirmed",
        "accessMode": "public_web_page",
        "accessVerifiedAt": "2026-08-30",
        "reviewedAt": "2026-08-30"
      }
    ],
    "applicationNumber": "FDA NDA 208658（SYNJARDY XR；恩格列净/盐酸二甲双胍缓释片）",
    "approvalTimeline": [
      {
        "date": "2016-12-10",
        "title": {
          "zh": "美国 SYNJARDY XR NDA 208658 营销记录起始",
          "en": "U.S. SYNJARDY XR NDA 208658 marketing record began"
        },
        "detail": {
          "zh": "当前 DailyMed 产品数据把 SYNJARDY XR、NDA 208658 和 2016-12-10 营销起始记录相连；标签同时列美国初始批准年份为 2015。该节点只建立美国产品史。",
          "en": "Current DailyMed product data link SYNJARDY XR, NDA 208658 and a 10 Dec 2016 marketing-start record; the label also lists 2015 as the initial U.S. approval year. This establishes U.S. product history only."
        },
        "source": {
          "id": "src_527bcad202bf135e",
          "label": "DailyMed（NLM）：SYNJARDY XR 当前美国公开标签（NDA 208658 与产品记录）",
          "url": "https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=8006ba29-ee3a-f852-a9bb-c8ec9b41cf66",
          "audience": "public",
          "reviewStatus": "approved",
          "publish": true,
          "documentStatus": "current_regulatory_record",
          "documentKind": "product_label",
          "market": "US",
          "accessStatus": "public_access_confirmed",
          "accessMode": "public_web_page",
          "accessVerifiedAt": "2026-08-30",
          "reviewedAt": "2026-08-30"
        }
      },
      {
        "date": "2026-08-21",
        "title": {
          "zh": "当前 DailyMed SPL v18 发布",
          "en": "Current DailyMed SPL v18 published"
        },
        "detail": {
          "zh": "该版本于 2026-08-11 更新、2026-08-21 发布，并在 2026-08 修订乳酸性酸中毒黑框警示。本页说明书阅读、准确包装、整片吞服及共同成分核对均以这一当前标签为主要来源。",
          "en": "This version was updated 11 Aug and published 21 Aug 2026, with the lactic-acidosis boxed warning revised in Aug 2026. This page's label reading, exact packages, whole-tablet rule and shared-ingredient review use that current label as the primary source."
        },
        "source": {
          "id": "src_527bcad202bf135e",
          "label": "DailyMed（NLM）：SYNJARDY XR 当前美国公开品牌标签（SPL v18；2026-08-21 发布）",
          "url": "https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=8006ba29-ee3a-f852-a9bb-c8ec9b41cf66",
          "audience": "public",
          "reviewStatus": "approved",
          "publish": true,
          "documentStatus": "current_regulatory_record",
          "documentKind": "product_label",
          "market": "US",
          "accessStatus": "public_access_confirmed",
          "accessMode": "public_web_page",
          "accessVerifiedAt": "2026-08-30",
          "reviewedAt": "2026-08-30"
        }
      }
    ],
    "marketStatus": [
      {
        "market": {
          "zh": "美国",
          "en": "United States"
        },
        "status": {
          "zh": "当前公开品牌标签与四种准确展示包装已建立",
          "en": "Current public brand label and four exact displayed packages established"
        },
        "detail": {
          "zh": "逐一记录四种每片双成分强度、NDC、瓶装数量、颜色、形状、刻印和官方标签面板；不表示具体渠道库存、购买资格、真伪或个人片数。",
          "en": "Records both per-tablet ingredient amounts, NDC, bottle count, colour, shape, imprint and official label panel for four displayed products. It does not establish channel stock, purchasing eligibility, authenticity or an individual tablet count."
        }
      },
      {
        "market": {
          "zh": "欧盟",
          "en": "European Union"
        },
        "status": {
          "zh": "当前 Synjardy 普通片产品资料已建立为分市场核对入口",
          "en": "Current Synjardy immediate-release product information established as a separate-market check"
        },
        "detail": {
          "zh": "EMA 当前资料列恩格列净 5/12.5 mg 与二甲双胍 850/1,000 mg 的普通片组合。它不是美国 SYNJARDY XR 的缓释片规格或替换表。",
          "en": "Current EMA material lists immediate-release combinations of empagliflozin 5/12.5 mg with metformin 850/1,000 mg. It is not a strength or substitution table for U.S. SYNJARDY XR extended-release tablets."
        }
      },
      {
        "market": {
          "zh": "中国大陆、日本及其他市场",
          "en": "Mainland China, Japan and other markets"
        },
        "status": {
          "zh": "待逐项建立现行监管产品记录",
          "en": "Current regulatory product records not established"
        },
        "detail": {
          "zh": "不从美国或欧盟商品名、共同成分、NDA/许可或包装推定当地批准、持有人、规格、供应、原研/参比关系或可替代性。",
          "en": "No local approval, holder, strength, supply, originator/reference relationship or interchangeability is inferred from a U.S. or EU trade name, shared ingredients, NDA/authorisation or pack."
        }
      }
    ],
    "frequentlyAskedQuestions": [
      {
        "question": {
          "zh": "10 mg/1,000 mg 是 1,010 mg，还是一天两个时间？",
          "en": "Does 10 mg/1,000 mg mean 1,010 mg, or two times of day?"
        },
        "answer": {
          "zh": "都不是。它表示一片分别含恩格列净 10 mg 和盐酸二甲双胍 1,000 mg。两个数字属于两种成分，不能相加后与其他药比较，也不能推导个人频次或片数。",
          "en": "Neither. One tablet contains 10 mg empagliflozin and 1,000 mg metformin HCl. The two numbers belong to two ingredients and cannot be added for comparison with another medicine or used to derive an individual's frequency or tablet count."
        }
      },
      {
        "question": {
          "zh": "药片太大，可以掰开、压碎、溶解或嚼碎吗？",
          "en": "Can a large tablet be split, crushed, dissolved or chewed?"
        },
        "answer": {
          "zh": "当前美国标签要求整片吞服，并明确不得掰开、压碎、溶解或咀嚼。吞咽困难时请带准确药盒联系开方团队或药师讨论可行产品，不要自行破坏缓释结构。",
          "en": "The current U.S. label requires swallowing whole and explicitly says not to split, crush, dissolve or chew. If swallowing is difficult, take the exact pack to the prescriber or pharmacist to discuss an appropriate product rather than damaging the extended-release design."
        }
      },
      {
        "question": {
          "zh": "已经吃 SYNJARDY XR，还能再吃 JARDIANCE 或二甲双胍吗？",
          "en": "Can JARDIANCE or metformin be added when SYNJARDY XR is already used?"
        },
        "answer": {
          "zh": "网页不能决定联用。SYNJARDY XR 已含恩格列净和盐酸二甲双胍；药单中再出现共同成分必须优先核对，不能自行叠加、轮换或停掉其中一盒。",
          "en": "A webpage cannot decide combination use. SYNJARDY XR already contains empagliflozin and metformin HCl. Another shared ingredient on the medicine list requires priority review, not self-combination, alternation or stopping a pack."
        }
      }
    ],
    "relatedMedicineChecks": [],
    "relatedArticleSlugs": [
      "medicine-label-for-everyday-questions",
      "dosage-forms-are-part-of-medicine-identity",
      "how-to-read-a-drug-label",
      "generic-drugs-and-bioequivalence"
    ]
  },
  "canonicalUrls": {
    "zh": "https://origindrug.com/drugs/synjardy-xr/",
    "en": "https://origindrug.com/en/drugs/synjardy-xr/"
  },
  "limitations": [
    "No originator, generic, interchangeability, availability, price, holder, strength or sale-eligibility conclusion is inferred beyond the linked source documents.",
    "Target-market current labels and official records must be checked separately."
  ]
}