What this pack is
DuoPlavin is the brand name in this record; clopidogrel and acetylsalicylic acid film-coated tablets is the generic name. Read both together with the dosage form (oral tablet).
PACK CHECK · MARKET FIRST
Clopidogrel's active metabolite irreversibly inhibits the platelet ADP P2Y12 pathway; aspirin irreversibly inhibits platelet cyclooxygenase and lowers thromboxane A2. The two pathways explain the fixed combination and why another antithrombotic medicine must not be added casually.
Read source: Europe ↗Current regulatory record · reviewed 2026-09-06More 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.
No source-verifiable mainland-China trade-name cue has been established for this record. This does not establish whether the medicine exists, is approved or is available in mainland China. Check pack text and current CDE/NMPA records item by item.
FOR EVERYDAY QUESTIONS
DuoPlavin is the brand name in this record; clopidogrel and acetylsalicylic acid film-coated tablets 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.
How to read a score line: ‘scored’ or ‘unscored’ first identifies this labelled presentation. A score line by itself does not permit self-splitting, reducing or changing the product. Only an explicit statement in the current label for this exact presentation, checked with a pharmacist against the prescription, can support any further handling.
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.
EU · Current EMA EU product information (updated 11 Jun 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.
EU · Current EMA EU product information (updated 11 Jun 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.
EU · Current EMA EU product information (updated 11 Jun 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.
EU · Current EMA EU product information (updated 11 Jun 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.
EU · Current EMA EU product information (updated 11 Jun 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.
EU · Current EMA EU product information (updated 11 Jun 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.
EU · Current EMA EU product information (updated 11 Jun 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.
EU · Current EMA EU product information (updated 11 Jun 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.
EU · Current EMA EU product information (updated 11 Jun 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.
EU · Current EMA EU product information (updated 11 Jun 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.
EU · Current EMA EU product information (updated 11 Jun 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.
EU · Current EMA EU product information (updated 11 Jun 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.
EU · Current EMA EU product information (updated 11 Jun 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.
EU · Current EMA EU product information (updated 11 Jun 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.
EU · Current EMA EU product information (updated 11 Jun 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
The 75/75 mg tablet is yellow and marked C75/A75; the 75/100 mg tablet is light pink and marked C75/A100. Colour, shape, imprint, blister or a web screenshot is only a clue and cannot establish authenticity; no similar pack substitutes for an unavailable exact official pack image.
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.
In 75/75 and 75/100, the first 75 mg is clopidogrel and the second figure is aspirin in that same tablet. The page explains ingredients, packs, warning signals and care boundaries; it does not generate individual tablet counts, stopping/switching, missed-use or perioperative plans.
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 DuoPlavin (clopidogrel and acetylsalicylic acid film-coated tablets). Keep the exact pack, its current label and the full medicine list together.
DuoPlavin is the brand in this record and clopidogrel and acetylsalicylic acid film-coated tablets is the active-ingredient name. Check both with the dosage form (DuoPlavin film-coated tablets combine clopidogrel 75 mg with aspirin 75 mg or 100 mg in one tablet. The two figures belong to two active ingredients, not one 150 mg or 175 mg medicine; this page does not infer splitting permission from the oval shape.) 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 DuoPlavin. 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
The current EMA EPAR lists 14 Mar 2010 as the authorisation date for DuoPlavin EMEA/H/C/001143.
EMA: current EU EPAR for DuoPlavin (EMEA/H/C/001143; product information updated 11 Jun 2026) ↗The current product information consolidates both strengths, warnings, interactions, excipients, appearance and pack authorisation numbers in one official document.
EMA: current EU DuoPlavin product information and electronic leaflet (75 mg/75 mg and 75 mg/100 mg; updated 11 Jun 2026) ↗EPAR, product information and public overview were checked item by item; the separate withdrawn application EMEA/H/C/000874 was not treated as the current product.
EMA: current EU EPAR for DuoPlavin (EMEA/H/C/001143; product information updated 11 Jun 2026) ↗MARKET SCOPE
Fifteen pack authorisation numbers come from current product information; not all pack sizes may be marketed, so authorisation numbers are not live inventory.
EU names, packs or shared ingredients do not establish local approval, brand, reference status, supply, reimbursement, price or interchangeability.
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. Seventy-five mg is clopidogrel and 100 mg is aspirin in that same tablet. The two active ingredients must remain separate and must not be summed for comparison with any 175 mg product.
Do not add one yourself. DuoPlavin already contains both ingredients. Have a pharmacist or clinician review every prescription, OTC product and pack, and do not self-stop when possible duplication is found.
A website cannot set the number of stopping days. Tell the responsible clinician and dentist in advance so they can balance the procedure, bleeding risk and thrombotic risk.
The label confirms a CYP2C19 role in clopidogrel activation and available genotype tests, but it does not support a website requiring whole-genome screening for everyone. The treating team should decide from the indication, prior events, interactions and local guidance.
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.