Plavix - 54569-4700-0 - (clopidogrel bisulfate)

Alphabetical Index


Drug Information of Plavix

Product NDC: 54569-4700
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: 54569-4700
Labeler Name: A-S Medication Solutions LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020839
Marketing Category: NDA
Start Marketing Date: 19990226

Package Information of Plavix

Package NDC: 54569-4700-0
Package Description: 30 TABLET, FILM COATED in 1 BOTTLE, DISPENSING (54569-4700-0)

NDC Information of Plavix

NDC Code 54569-4700-0
Proprietary Name Plavix
Package Description 30 TABLET, FILM COATED in 1 BOTTLE, DISPENSING (54569-4700-0)
Product NDC 54569-4700
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name clopidogrel bisulfate
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 19990226
Marketing Category Name NDA
Labeler Name A-S Medication Solutions 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 Plavix


General Information