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) |
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 NDC: | 54569-4700-2 |
Package Description: | 90 TABLET, FILM COATED in 1 BOTTLE, DISPENSING (54569-4700-2) |
NDC Code | 54569-4700-2 |
Proprietary Name | Plavix |
Package Description | 90 TABLET, FILM COATED in 1 BOTTLE, DISPENSING (54569-4700-2) |
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] |