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Clopidogrel bisulfate
Clopidogrel bisulfate - 55111-671-31 - (Clopidogrel bisulfate)
Drug Information of Clopidogrel bisulfate
| Product NDC: | 55111-671 |
| Proprietary Name: | Clopidogrel bisulfate |
| Non Proprietary Name: | Clopidogrel bisulfate |
| Active Ingredient(s): | 300 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: | 55111-671 |
| Labeler Name: | Dr.Reddy's Laboratories Limited |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA091023 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20120517 |
Package Information of Clopidogrel bisulfate
| Package NDC: | 55111-671-31 |
| Package Description: | 5 BLISTER PACK in 1 CARTON (55111-671-31) > 6 TABLET, FILM COATED in 1 BLISTER PACK (55111-671-06) |
NDC Information of Clopidogrel bisulfate
| NDC Code | 55111-671-31 |
| Proprietary Name | Clopidogrel bisulfate |
| Package Description | 5 BLISTER PACK in 1 CARTON (55111-671-31) > 6 TABLET, FILM COATED in 1 BLISTER PACK (55111-671-06) |
| Product NDC | 55111-671 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Clopidogrel bisulfate |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 20120517 |
| Marketing Category Name | ANDA |
| Labeler Name | Dr.Reddy's Laboratories Limited |
| Substance Name | CLOPIDOGREL BISULFATE |
| Strength Number | 300 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Decreased Platelet Aggregation [PE],P2Y12 Platelet Inhibitor [EPC],P2Y12 Receptor Antagonists [MoA] |
