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Clopidogrel Bisulfate - 47335-894-13 - (Clopidogrel Bisulfate)

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Drug Information of Clopidogrel Bisulfate

Product NDC: 47335-894
Proprietary Name: Clopidogrel Bisulfate
Non Proprietary Name: Clopidogrel Bisulfate
Active Ingredient(s): 75    mg/1 & nbsp;   Clopidogrel Bisulfate
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Clopidogrel Bisulfate

Product NDC: 47335-894
Labeler Name: Sun Pharma Global FZE
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA090494
Marketing Category: ANDA
Start Marketing Date: 20120518

Package Information of Clopidogrel Bisulfate

Package NDC: 47335-894-13
Package Description: 500 TABLET, FILM COATED in 1 BOTTLE (47335-894-13)

NDC Information of Clopidogrel Bisulfate

NDC Code 47335-894-13
Proprietary Name Clopidogrel Bisulfate
Package Description 500 TABLET, FILM COATED in 1 BOTTLE (47335-894-13)
Product NDC 47335-894
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Clopidogrel Bisulfate
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20120518
Marketing Category Name ANDA
Labeler Name Sun Pharma Global FZE
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 Bisulfate


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