PLAVIX

This brand name is authorized in Austria, Brazil, Canada, Cyprus, Germany, Ecuador, Estonia, Spain, Finland, France, Hong Kong, Croatia, Ireland, Israel, Italy, Japan, Lithuania, Mexico, Netherlands, Poland, Romania, Singapore, Tunisia, Turkey, United Kingdom, United States, South Africa

Active ingredients

The drug PLAVIX contains one active pharmaceutical ingredient (API):

1 Clopidogrel UNII 08I79HTP27 - CLOPIDOGREL BISULFATE

Clopidogrel is a prodrug, one of whose metabolites is an inhibitor of platelet aggregation. Clopidogrel must be metabolised by CYP450 enzymes to produce the active metabolite that inhibits platelet aggregation. Read about Clopidogrel

Medication package inserts

Below package inserts are available for further reading:

Title	Information Source	Document Type
PLAVIX Film-coated tablet	FDA, National Drug Code (US)	MPI, US: SPL/PLR
PLAVIX 75mg Film-coated tablet	Medicines & Healthcare Products Regulatory Agency (GB)	MPI, EU: SmPC

Medicine classification

This drug has been classified in the anatomical therapeutic chemical (ATC) classification system as follows:

ATC code	Group title	Classification
B01AC04	Clopidogrel	B Blood and blood forming organs → B01 Antithrombotic agents → B01A Antithrombotic agents → B01AC Platelet aggregation inhibitors excl. heparin
Discover more medicines within B01AC04

Authorization and marketing

This drug has been assigned below unique identifiers within the countries it is being marketed:

Country	Identification scheme	Identifier(s)
Country: BR	Câmara de Regulação do Mercado de Medicamentos	Identifier(s): 576720030058817
Country: CA	Health Products and Food Branch	Identifier(s): 02238682
Country: DE	Bundesinstitut für Arzneimittel und Medizinprodukte	Identifier(s): 00051055, 00262119, 00276995, 00549105, 00956187, 01037040, 01146906, 01236905, 01423292, 01501997, 01737530, 01813774, 02418910, 04129423, 04408100, 04412544, 04551033, 06326292, 07770764, 07770770, 09629082, 10227897, 10947189, 16529518, 16817660
Country: EC	Agencia Nacional de Regulación, Control y Vigilancia Sanitaria	Identifier(s): 22.734-1-09-06
Country: EE	Ravimiamet	Identifier(s): 1040588, 1065732, 1065743, 1131118, 1304941, 1304952, 1304963, 1364622, 1364633, 1364644, 1471395, 1471407
Country: ES	Centro de información online de medicamentos de la AEMPS	Identifier(s): 98069001, 98069001AIP, 98069001AIP3, 98069002, 98069009
Country: FI	Lääkealan turvallisuus- ja kehittämiskeskus	Identifier(s): 020847, 124119, 511832
Country: FR	Base de données publique des médicaments	Identifier(s): 60562855, 63564053
Country: GB	Medicines & Healthcare Products Regulatory Agency	Identifier(s): 121843, 136636, 139459, 147215, 375286, 375289, 376935, 381632
Country: HK	Department of Health Drug Office	Identifier(s): 43787, 57453
Country: IE	Health Products Regulatory Authority	Identifier(s): 40901, 41021, 41080, 41086, 41095
Country: IL	מִשְׂרַד הַבְּרִיאוּת	Identifier(s): 3779
Country: IT	Agenzia del Farmaco	Identifier(s): 034128013, 043220019, 043976012, 044418010, 044667018, 044811014, 049461015
Country: JP	医薬品医療機器総合機構	Identifier(s): 3399008F1025, 3399008F2021
Country: LT	Valstybinė vaistų kontrolės tarnyba	Identifier(s): 1003137, 1005409, 1008163, 1008164, 1030244, 1030245, 1030246, 1030248, 1030249, 1030250, 1030251, 1030252, 1030253, 1030254, 1032122, 1032123, 1032124, 1056121, 1056122, 1064250
Country: MX	Comisión Federal para la Protección contra Riesgos Sanitarios	Identifier(s): 474M98
Country: NL	Z-Index G-Standaard, PRK	Identifier(s): 124559, 124567
Country: PL	Rejestru Produktów Leczniczych	Identifier(s): 100084778, 100192769
Country: RO	Agenția Națională a Medicamentului și a Dispozitivelor Medicale	Identifier(s): W69341001, W69341006, W69341007, W69341008, W69341009, W69341010, W69341011, W69341012, W69341013, W69341014, W69341015, W69341016, W69341017, W69341018, W69341019, W69341020
Country: SG	Health Sciences Authority	Identifier(s): 09828P, 14332P
Country: TN	Direction de la Pharmacie et du Médicament	Identifier(s): 3723023H, 9263241
Country: TR	İlaç ve Tıbbi Cihaz Kurumu	Identifier(s): 8699809097698, 8699809098190
Country: US	FDA, National Drug Code	Identifier(s): 0024-1171, 0024-1332, 55289-911, 63653-1171, 63653-1332
Country: ZA	Health Products Regulatory Authority	Identifier(s): 36/8.2/0408