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Clopidogrel - 64679-314-02 - (Clopidogrel)

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Drug Information of Clopidogrel

Product NDC: 64679-314
Proprietary Name: Clopidogrel
Non Proprietary Name: Clopidogrel
Active Ingredient(s): 75    mg/1 & nbsp;   Clopidogrel
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Clopidogrel

Product NDC: 64679-314
Labeler Name: Wockhardt USA LLC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA202266
Marketing Category: ANDA
Start Marketing Date: 20120522

Package Information of Clopidogrel

Package NDC: 64679-314-02
Package Description: 90 TABLET, FILM COATED in 1 BOTTLE (64679-314-02)

NDC Information of Clopidogrel

NDC Code 64679-314-02
Proprietary Name Clopidogrel
Package Description 90 TABLET, FILM COATED in 1 BOTTLE (64679-314-02)
Product NDC 64679-314
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Clopidogrel
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20120522
Marketing Category Name ANDA
Labeler Name Wockhardt USA LLC.
Substance Name CLOPIDOGREL BISULFATE
Strength Number 75
Strength Unit mg/1
Pharmaceutical Classes Decreased Platelet Aggregation [PE],P2Y12 Platelet Inhibitor [EPC],P2Y12 Receptor Antagonists [MoA]

Complete Information of Clopidogrel


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