What this pack is
Celebrex is the brand name in this record; celecoxib is the generic name. Read both together with the dosage form (oral capsule).
PACK CHECK · MARKET FIRST
CelebrexGeneric namecelecoxib
Mainland China pack-name cue西乐葆®Historical or public source cue · verify the current target-market record · Open reference ↗
How this medicine works
The DailyMed CELEBREX historical label describes celecoxib as a nonsteroidal anti-inflammatory drug (NSAID) and points to selective inhibition of cyclooxygenase-2 (COX-2). This explains a pharmacologic pathway; it does not predict individual suitability, cause of pain, amount, combination, switching or stopping.
Read source: United States ↗reviewed 2026-08-20More about its action and precautions →Check the market, names, dosage form and route together
A medicine may use different brand names across markets. Keep the market, brand, generic name, dosage form and route together; one matching field does not prove that two packs are the same or interchangeable.
Open the complete product-identity record
Use these fields when the pack, market name or package image needs closer checking. They are evidence boundaries, not substitution instructions.
- Mainland China pack-name cue
- 西乐葆®
- International brand name
- Celebrex
- Generic name
- celecoxib
- Dosage-form class
- Dosage form and presentation as documented in the linked primary label
- Route
- Oral
- Package-image status
- A source-linked public label image is available below
Mainland China trade-name search cue:西乐葆®. This is a historical/public cue for reading pack text. It does not establish current approval, holder, supply or sale eligibility. Open reference ↗
FOR EVERYDAY QUESTIONS
After the leaflet, continue with the question you still need to check
What this page can show
This is a source-traceable public record. It helps you read the product identity and its listed source documents; each market still needs its own current record check.
What to bring to the next conversation
Bring the actual pack, the label or prescription, and a complete medicine list when you speak with a pharmacist or clinician.
NEXT SAFE STEP
Choose the next safe check
A question about changing, combining or splitting?Put the exact packs on one list before a pharmacist or prescriber checks the full context.Open the family medicine list →A question about cost, reimbursement or availability?First lock the market, exact presentation and date. Use local official reimbursement, hospital or pharmacy channels for a current answer rather than a web estimate.Open regulator and market-record entry points →Unsure about a pack or a cross-border product?Photo reading can return possible record matches only. Check the actual product against the current regulator record for its market.Identify pack text locally →Saw a recall, approval or procurement headline?Open the original publisher, then match its product, market and date. Do not make a stop or switch decision from a headline.Read primary-source news →
PRODUCT PRESENTATION IDENTITY
Strength, pack and device identity
Package strength is not an individual dose. These fields help identify the exact labelled product; they do not calculate how much, how often, a missed-use action, splitting, switching or conversion.
1 source-backed strength, pack or device records — open the full list
First match the market, dosage form and labelled amount on the pack in hand. The number of tablets, sachets or devices in a pack is not a personal dose or schedule.
United States label · DailyMed public label (2025 package artwork; source checked 23 Aug 2026)
Celecoxib 100 mg per capsule; 100-capsule bottle
- Product code
- NDC 58151-083-01
- Form and route
- CELEBREX celecoxib oral capsule · oral
- Container
- 100-capsule bottle
- Listing review
- Current label display and NDC Directory listing reviewed 2026-08-23; actual marketing, stock and availability are not established.
- celecoxib
- 100 mglabelled amount per capsule; not an individual's capsule count, combination, adjustment or switching rule
- Package
- 100 capsules per bottle
- Labelled appearance
- white capsule with blue bands on body and cap; bottle-label display panel · hard capsule; imprint 7767 / 100
PUBLIC LABEL IMAGE
Appearance and package-text clues
This current public-label package panel helps check the brand, generic name, strength and dosage-form clues only. It does not authenticate a product in hand or establish originator status, availability, sale eligibility, another package or another market.
Open the public label source ↗LABEL READING · NOT A PRESCRIPTION
CELEBREX label reading: keep the capsule, milligram strength and related medicines distinct
Reading level: drug-specific label reading. This record has been expanded around its dosage form or a higher-risk reading question; the current target-market label and professional review still apply.
This module uses the Pfizer 2021 U.S. FDA and DailyMed CELEBREX label archives as reading entry points. It helps check CELEBREX, celecoxib, oral capsules, 50/100/200/400 mg and warning language; it does not provide an individual dose, pain plan, combination, switch or stopping advice.
- First check CELEBREX, celecoxib, oral capsule, target market and stated strength per capsule. 50, 100, 200 and 400 mg first identify products listed in the historical label; they are not an answer to “how many today,” and do not permit self-combining strengths, substitution or use of someone else’s prescription.
- The historical label flags questions that can require professional review with related NSAIDs, salicylates and multiple medicines. Do not self-combine, alternate or add aspirin merely because packages say “pain” or “inflammation” or belong to a related class; bring actual packages and the complete medicine list for item-by-item pharmacist or clinician review.
- The historical FDA/DailyMed labels contain serious cardiovascular and gastrointestinal warnings and state that older people and those with a prior peptic-ulcer or GI-bleeding history are at higher risk for serious GI events. With black stools, vomiting blood, chest discomfort, breathing trouble, fainting or another acute severe concern, use timely local urgent medical support rather than self-adjusting or switching from a webpage.
- Whether a capsule may be opened, sprinkled on food, mixed, or managed after a missed dose must be confirmed item by item from the exact product, target market’s current label, actual pack and pharmacist advice. Even if a historical label records one capsule-handling method, it cannot be generalised to another strength, brand, capsule or market product.
PHARMACOVIGILANCE · OFFICIAL ROUTES
Check safety information in the right market
Start with the public label or product record linked to this dossier, then use the official safety routes below for the market that applies to the medicine in hand.
Match five details before using a safety record
- Brand and generic nameBoth must match the medicine named by the record.
- Dosage form and strengthTablet, capsule, injection, inhaler, patch and eye drop are not interchangeable.
- Market and notice dateA record applies only to the country or region and date it names.
- Lot, pack and manufacturerRecord these only when the official notice specifically names them.
- Current product informationA historical record may have been superseded by the current label.
This checklist only helps organise the right question. It does not create a personal conclusion about stopping, switching, dose, combination or suitability.
This dossier’s product-level source checkFDA · United States · Regulatory product record or label archive · 2026-08-20
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.
Markets actually represented by the reviewed product documents
- United States · 3
This is a document-coverage summary, not a claim that the medicine is authorised, supplied, interchangeable or actively monitored in every listed market today.
This record’s label or product-record routeFDA: CELEBREX 2021 U.S. prescribing information (NDA 020998) ↗Historical public record · reviewed 2026-08-20
Other official market or version documents for this record
These are separately reviewed product documents for the same dossier. Their market, date, dosage form and document status must stay attached to each link; they do not establish interchangeability between products, strengths, packs, indications or countries.
- U.S. National Library of Medicine DailyMed · United States · Public medicine label · 2026-08-20DailyMed (NLM): CELEBREX celecoxib 100 mg / 100-capsule-bottle U.S. public label panel (Viatris; 2025 package artwork) ↗reviewed 2026-08-20
- U.S. National Library of Medicine DailyMed · United States · Public medicine label · 2026-08-20DailyMed (NLM): CELEBREX public historical-label archive (Pfizer, 2021-04 updated) ↗reviewed 2026-08-20
Reviewed official safety records
A dated record is not automatically a current alert. Read the named product, form, batch, market, date and source type before treating it as relevant.
- FDA Drug Safety Communication: NSAID risk communication in pregnancy at about 20 weeks or later, including celecoxib2020-10-15 · On 2020-10-15, FDA issued an NSAID Drug Safety Communication whose product table explicitly lists celecoxib/Celebrex. It says NSAID use at about 20 weeks of pregnancy or later may be associated with fetal kidney problems and low amniotic fluid, and describes related U.S. prescribing-information updates. This is a dated U.S. class regulatory communication; it does not establish that any person has a problem or support self-starting, stopping, switching, reducing, or replacing pain medicine. Pregnancy, suspected pregnancy, or pain-medicine questions require review of the exact product, current label for the relevant market, and complete medicine list with the prescribing team or pharmacist.Primary-source record (open linked document) ↗reviewed 2026-08-22
Global official safety gateways
- NMPA Centre for Drug Reevaluation · Mainland ChinaPrimary 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.Drug-vigilance bulletins and safety notices ↗reviewed 2026-08-22
- FDA · United StatesPrimary FDA pages for important new safety issues, labelling changes and risk communications.Drug Safety Communications ↗reviewed 2026-08-22
- FDA MedWatch · United StatesU.S. MedWatch safety-information and reporting gateway; a report does not itself establish causality.Safety information and serious-problem reporting ↗reviewed 2026-08-22
- EMA · European Union / European Economic AreaOfficial EU gateway for pharmacovigilance, suspected adverse-reaction reports and PRAC safety assessment.Pharmacovigilance overview and EudraVigilance ↗reviewed 2026-08-22
- MHRA · United KingdomPrimary UK MHRA medicine-safety updates for professionals and the public.Drug Safety Update ↗reviewed 2026-08-22
- PMDA · JapanPMDA’s English official safety gateway; exact products still require checking against the Japanese product page and current documents.Medicine safety information ↗reviewed 2026-08-22
- MFDS · Republic of KoreaMFDS’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.Medicine safety letters ↗reviewed 2026-08-22
- HSA · SingaporeHSA’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.Adverse-event reporting and medicine-safety information ↗reviewed 2026-08-22
- Health Canada · CanadaHealth 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.MedEffect Canada: advisories, warnings and recalls ↗reviewed 2026-08-22
- TGA · AustraliaPrimary Australian TGA safety alerts, advisories and monitoring information for therapeutic products.Medicine safety alerts ↗reviewed 2026-08-22
- Swissmedic · SwitzerlandOfficial Swissmedic gateway for pharmacovigilance, signal assessment and suspected adverse-reaction reporting; a report or signal does not itself confirm individual causality.Pharmacovigilance and suspected adverse-reaction reporting ↗reviewed 2026-08-22
- Medsafe · New ZealandNew Zealand Medsafe gateway for public and professional medicine safety communications and archives; older notices may have been superseded by current product information.Medicine safety communications ↗reviewed 2026-08-22
- SAHPRA · South AfricaSAHPRA’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.Medicine safety information, alerts and pharmacovigilance ↗reviewed 2026-08-22
- WHO · GlobalWHO’s cross-market safety-alert archive; every historical notice must be read against its date, named product and market.Medicine and vaccine safety-alert archive ↗reviewed 2026-08-22
- Anvisa · BrazilAnvisa’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.Pharmacovigilance, alerts and VigiMed ↗reviewed 2026-08-22
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.
For severe or rapidly worsening symptoms, suspected overdose, a severe allergic reaction, loss of consciousness or another emergency, use local emergency services. Do not wait for an online alert search or change a medicine from this page.
PRIVATE FAMILY LIST
Bring this record into a local medicine list
Only the brand, generic name, dosage form and route are added, and they stay in this browser. Copy strength, label directions, start/stop history and any concern from the actual pack; this tool does not calculate a dose or decide combination, switching or stopping.
Add to the family medicine list →PACK · LABEL · MEDICINE LIST
Six checks for this medicine pack
Use this card to organise questions about Celebrex (celecoxib). Keep the exact pack, its current label and the full medicine list together.
Identify the exact product
Celebrex is the brand in this record and celecoxib is the active-ingredient name. Check both with the dosage form (Dosage form and presentation as documented in the linked primary label) and the market on the actual pack.
Read the labelled strength in context
mg, mcg, mg/mL or a percentage describes the labelled amount in one tablet, capsule, measured volume, spray or other unit. It is not an answer to how many units a person should take.
Check before splitting or opening
Before splitting, crushing, chewing or opening anything, find an explicit instruction for this exact product in its current label and ask a pharmacist. A score line or a previous pack is not enough by itself.
Put every product on one list
Include prescriptions, over-the-counter products, eye drops, creams, vitamins, minerals, herbs and supplements. A pharmacist or prescriber needs the whole list before any combination, alternation, switch or stop is considered.
Ask a specific pharmacogenetics question
Ask which medicine, which gene and what clinical decision a result could change. A gene–drug association does not mean broad genetic testing is needed for everyone and must not be used to change treatment without professional review.
Know when to seek urgent help
For a suspected overdose, a severe allergic reaction, fainting or difficulty breathing, use the local emergency or poison-information service now. Do not wait for a website reply or alter several medicines to test what caused it.
This card does not calculate a dose, decide whether medicines can be combined, or replace a clinician or pharmacist. Market-specific current labels and the person's full context still need review.
MARKET DOCUMENTS · READ SEPARATELY
Enlarged market leaflets and regulator documents
Each link retains its own market, date, dosage form and document status. These documents support larger-print reading and item-by-item checking; they do not make products, strengths, packs, indications or use between countries or regions interchangeable.
- FDA: CELEBREX 2021 U.S. prescribing information (NDA 020998) ↗Historical public record · reviewed 2026-08-20
- DailyMed (NLM): CELEBREX celecoxib 100 mg / 100-capsule-bottle U.S. public label panel (Viatris; 2025 package artwork) ↗reviewed 2026-08-20
- DailyMed (NLM): CELEBREX public historical-label archive (Pfizer, 2021-04 updated) ↗reviewed 2026-08-20
HOW IT WORKS · NOT A TREATMENT PLAN
How celecoxib works: the label describes a selective COX-2 inhibitor
- “Selective COX-2” or “NSAID” is not a tool for deciding whether a pain problem needs medicine, which pain medicine to select or whether products can be combined on the same day. Cause, history, all medicines, dosage form and current label need professional review together.
- A shared anti-inflammatory or pain pathway does not make CELEBREX self-combinable, alternatable or substitutable with another NSAID, a salicylate-containing product or a combination cold/pain product. A mechanism page cannot complete an interaction review.
- Mechanism cannot turn 50, 100, 200 or 400 mg capsules into a personal increase, decrease, long-term-use or stopping rule. With a contemplated change, multiple medicines or a new symptom, bring actual packages and the complete medicine list to local pharmacist, clinician or urgent support.
SOURCE EVIDENCE REGISTER
Source evidence map
Every public link is labelled with its market, document status and document type. A historical public record is not a current label, and an official lookup entry is not a product-specific record.
- DailyMed (NLM): CELEBREX celecoxib 100 mg / 100-capsule-bottle U.S. public label panel (Viatris; 2025 package artwork) ↗reviewed 2026-08-20
- FDA: CELEBREX 2021 U.S. prescribing information (NDA 020998) ↗Historical public record · reviewed 2026-08-20
- DailyMed (NLM): CELEBREX public historical-label archive (Pfizer, 2021-04 updated) ↗reviewed 2026-08-20
- FDA Drugs@FDA official search entry ↗Official lookup entry · reviewed 2026-08-20
SOURCE-TRACEABLE ARCHIVE
Celebrexcelecoxib
This page includes an exact current U.S. public-label package panel for Celebrex, alongside documentary primary-source material. It helps check product identity, but does not itself establish originator status, product quality, availability or sale eligibility.
DOCUMENT TIMELINE
Document timeline
Initial U.S. approval year listed in the FDA label
The FDA label archive linked here lists Initial U.S. Approval: 1998. This historical locator is not a conclusion about current approval, availability, holder or another market.
FDA: CELEBREX label archive ↗FDA label archive version
This page links the 2021 FDA label archive as a traceable reading entry point. Current labeling, strength, indication and safety information require separate verification against the target market’s current document.
FDA: CELEBREX label archive ↗
MARKET SCOPE
Market-record boundary
United States
Public label archive linkedOnly the FDA document listed on this page is linked.
Mainland China, EU, Japan
Market record not establishedNo local approval, holder, strength, supply or sale-eligibility conclusion is inferred from the U.S. label archive.
How to read this record
Read each document in its stated market, date and dosage-form context. A historical record is not a current label and does not support individual medical, substitution or purchasing conclusions.
Keep international and mainland China records separate
This page has a U.S. public history/regulatory archive but no mainland China record for this specific product. That does not establish whether the medicine exists, is approved or is available in mainland China. Verify product identity, dosage form, strength, holder and the current label item by item.
Mainland China trade-name search cue: 西乐葆®
This cue helps read packaging and search official records. It does not establish current approval, holder, strength, originator relationship, supply or sale eligibility. Open historical reference ↗
RECORD FAQ
Record questions
Does a label archive represent current product information?
Not automatically. The archive locates a source; each point needs verification against the target market’s current official label.
Why are price and originator/generic conclusions not shown?
Those conclusions require separately complete and human-reviewed product, dosage-form, strength, pack, market, date and primary-record fields; one label file is insufficient.
READ NEXT
Related reading
Evidence status
The listed links are public sources selected for traceability. They must be rechecked against the current target-market record before any use beyond reading and research.