Product NDC: | 54868-6336 |
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) |
Product NDC: | 54868-6336 |
Labeler Name: | Physicians Total Care, Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA076273 |
Marketing Category: | ANDA |
Start Marketing Date: | 20120525 |
Package NDC: | 54868-6336-0 |
Package Description: | 30 TABLET, FILM COATED in 1 BOTTLE (54868-6336-0) |
NDC Code | 54868-6336-0 |
Proprietary Name | Clopidogrel bisulfate |
Package Description | 30 TABLET, FILM COATED in 1 BOTTLE (54868-6336-0) |
Product NDC | 54868-6336 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Clopidogrel bisulfate |
Dosage Form Name | TABLET, FILM COATED |
Route Name | ORAL |
Start Marketing Date | 20120525 |
Marketing Category Name | ANDA |
Labeler Name | Physicians Total Care, Inc. |
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] |