Plavix - 63653-1171-5 - (clopidogrel bisulfate)

Alphabetical Index


Drug Information of Plavix

Product NDC: 63653-1171
Proprietary Name: Plavix
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 Plavix

Product NDC: 63653-1171
Labeler Name: Bristol-Myers Squibb/Sanofi Pharmaceuticals Partnership
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020839
Marketing Category: NDA
Start Marketing Date: 19000101

Package Information of Plavix

Package NDC: 63653-1171-5
Package Description: 500 TABLET, FILM COATED in 1 BOTTLE (63653-1171-5)

NDC Information of Plavix

NDC Code 63653-1171-5
Proprietary Name Plavix
Package Description 500 TABLET, FILM COATED in 1 BOTTLE (63653-1171-5)
Product NDC 63653-1171
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name clopidogrel bisulfate
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 19000101
Marketing Category Name NDA
Labeler Name Bristol-Myers Squibb/Sanofi Pharmaceuticals Partnership
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 Plavix


General Information