NDC product
Clotrimazole and Betamethasone Dipropionate
NDC 0472-0379 · Actavis Pharma, Inc.
Key facts
| Product NDC | 0472-0379 |
|---|---|
| Proprietary name | Clotrimazole and Betamethasone Dipropionate |
| Nonproprietary name | Clotrimazole and Betamethasone Dipropionate |
| Substances | CLOTRIMAZOLE, BETAMETHASONE DIPROPIONATE |
| Dosage form | CREAM |
| Route | TOPICAL |
| Labeler | Actavis Pharma, Inc. |
| Product type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Application number | ANDA076002 |
| Pharmacologic classes | Azole Antifungal [EPC], Azoles [CS], Corticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC] |
| Marketing start | Dec 16, 2003 |
| 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: