NDC 68084-752
Clopidogrel
Clopidogrel Bisulfate
Clopidogrel is a Oral Tablet, Film Coated in the Human Prescription Drug category. It is labeled and distributed by American Health Packaging. The primary component is Clopidogrel Bisulfate.
| Product ID | 68084-752_84eb7545-2166-0960-e053-2991aa0a902a |
| NDC | 68084-752 |
| Product Type | Human Prescription Drug |
| Proprietary Name | Clopidogrel |
| Generic Name | Clopidogrel Bisulfate |
| Dosage Form | Tablet, Film Coated |
| Route of Administration | ORAL |
| Marketing Start Date | 2014-03-28 |
| Marketing Category | ANDA / ANDA |
| Application Number | ANDA076274 |
| Labeler Name | American Health Packaging |
| Substance Name | CLOPIDOGREL BISULFATE |
| Active Ingredient Strength | 300 mg/1 |
| Pharm Classes | Decreased Platelet Aggregation [PE],P2Y12 Platelet Inhibitor [EPC],P2Y12 Receptor Antagonists [MoA],Cytochrome P450 2C8 Inhibitors [MoA] |
| NDC Exclude Flag | N |
| Listing Certified Through | 2020-12-31 |