What this pack is
DIAMICRON MR is the brand name in this record; gliclazide is the generic name. Read both together with the dosage form (oral tablet).
PACK CHECK · MARKET FIRST
Mainland China pack-name cue达美康®Historical or public source cue · verify the current target-market record · Open reference ↗
TGA-released DIAMICRON MR product information describes gliclazide as an oral sulfonylurea that can lower blood glucose by stimulating insulin secretion from pancreatic beta cells. This explains an active-ingredient pathway only. The exact product identity in this dossier remains the DIAMICRON 60 mg MR modified-release tablet in ARTG 154042; mechanism does not determine anyone's glucose, suitability, tablet count, meals, co-use, pausing or substitution.
Read source: Australia ↗Historical public record · reviewed 2026-08-28More about its action and precautions →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.
Use these fields when the pack, market name or package image needs closer checking. They are evidence boundaries, not substitution instructions.
The evidence status and note below apply only to the stated market and source. They do not prove that packs in different markets can be substituted.
Mainland China trade-name search cue:达美康®. 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
DIAMICRON MR is the brand name in this record; gliclazide is the generic name. Read both together with the dosage form (oral tablet).
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.
Bring the actual pack, the label or prescription, and a complete medicine list when you speak with a pharmacist or clinician.
NEXT SAFE STEP
PRODUCT PRESENTATION 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.
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.
AU · TGA ARTG 154042 (verified 26 Aug 2026)
Source-text identity card: no displayable exact official package image. The fields below come from the cited label and are not a visual authentication result.
PACKAGE-VISUAL STATUS
This dossier retains DIAMICRON 60 mg MR, gliclazide 60 mg tablets, the MR modified-release form, blister packaging and PI/CMI routes in TGA ARTG 154042. No official package image that can be matched one-to-one to this exact ARTG presentation was retained; to avoid treating a retail image, version-uncertain image, another-market image or immediate-release-tablet image as an exact DIAMICRON MR package, the page withholds package imagery and retains the official electronic leaflets for enlarged reading.
LABEL READING · NOT A PRESCRIPTION
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 reads only DIAMICRON 60 mg MR, gliclazide, 60 mg per tablet, modified-release form and blister packaging in TGA ARTG 154042 and its official PI/CMI routes. It provides no individual tablet count, start, missed-use handling, meals, splitting, crushing, co-use, stopping, switching or purchase plan.
PHARMACOVIGILANCE · OFFICIAL ROUTES
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.
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 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.
This is a document-coverage summary, not a claim that the medicine is authorised, supplied, interchangeable or actively monitored in every listed market today.
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.
This is not a conclusion that the medicine has no risk, warning, recall or newer notice in another market. Start with the checked product-level label above, then use the official market gateways below for the product in hand.
See the reviewed safety-record directory →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
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
Use this card to organise questions about DIAMICRON MR (gliclazide). Keep the exact pack, its current label and the full medicine list together.
DIAMICRON MR is the brand in this record and gliclazide is the active-ingredient name. Check both with the dosage form (Gliclazide 60 mg MR (modified release) oral tablet; blister pack as listed in TGA ARTG 154042) and the market on the actual pack.
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.
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.
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 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.
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
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.
HOW IT WORKS · NOT A TREATMENT PLAN
SOURCE EVIDENCE REGISTER
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.
SOURCE-TRACEABLE ARCHIVE
This page links to public primary-source material for DIAMICRON MR. The archive is historical or documentary evidence only; it does not by itself establish originator status, product quality, current labelling, availability or sale eligibility.
DOCUMENT TIMELINE
TGA ARTG 154042 lists 11 Nov 2009 as the ARTG date for DIAMICRON 60 mg MR gliclazide 60 mg tablet blister pack. This date locates only this Australian regulatory product record; it does not establish approval, supply, sale eligibility, originator/generic relationship or individual suitability in another market.
Australian TGA: DIAMICRON 60 mg MR (ARTG 154042) ↗This review confirmed that TGA ARTG 154042 links to this product's Product Information (PI) and Consumer Medicine Information (CMI) routes. The PI/CMI are supplied to TGA by the relevant sponsor for publication; this page presents them only as primary reading routes and does not turn them into individual tablet-count, stopping, switching or purchase conclusions.
Australian TGA eBS: DIAMICRON 60 mg MR PI/CMI official entry routes ↗MARKET SCOPE
This page records only DIAMICRON 60 mg MR, gliclazide 60 mg tablets, the MR modified-release form and blister packaging in ARTG 154042; it does not authenticate a product or establish actual marketing, stock, purchase, individual tablet count, co-use, stopping, switching or interchangeability.
No local trade name, approval, packaging, supply, sale eligibility, originator/generic relationship or interchangeability is inferred from the Australian ARTG name, date, sponsor, PI/CMI or blister pack; every market requires separate checking against current local regulatory material.
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.
RECORD FAQ
No. These fields identify only the exact Australian modified-release tablet in TGA ARTG 154042. A shared generic name, nearby mg number, similar brand or package wording does not establish self-initiation, increase, make-up use, splitting, crushing, stopping, co-use, alternation or substitution; have a pharmacist or prescriber review the actual pack, current prescription and complete medicine list.
The PI/CMI are official primary reading routes for this exact product, but treatment decisions require the prescription, actual pack, other medicines, prior reactions and health status to be reviewed together. Do not self-stop, switch, increase, reduce or separate timing from a webpage, headline or one leaflet section alone.
READ NEXT
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.