NDC product
Clopidogrel bisulfate
NDC 0615-8625 · NCS HealthCare of KY, LLC dba Vangard Labs
Key facts
| Product NDC | 0615-8625 |
|---|---|
| Proprietary name | Clopidogrel bisulfate |
| Nonproprietary name | Clopidogrel bisulfate |
| Substances | CLOPIDOGREL BISULFATE |
| Dosage form | TABLET, FILM COATED |
| Route | ORAL |
| Labeler | NCS HealthCare of KY, LLC dba Vangard Labs |
| Product type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Application number | ANDA204165 |
| Pharmacologic classes | Cytochrome P450 2C8 Inhibitors [MoA], Decreased Platelet Aggregation [PE], P2Y12 Platelet Inhibitor [EPC], P2Y12 Receptor Antagonists [MoA] |
| Marketing start | Sep 15, 2015 |
| Listing certified through | Dec 31, 2027 |
At a glance
- 1–9 Package NDCs
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About National Drug Codes (NDC)
The National Drug Code (NDC) is the FDA's product identifier for drugs; the product NDC identifies the labeler and product, and each package adds a package code.
Source: U.S. Food and Drug Administration (FDA), National Drug Code Directory · Source date: