NDC product
calcipotriene and betamethasone dipropionate
NDC 0713-0848 · Cosette Pharmaceuticals, Inc.
Key facts
| Product NDC | 0713-0848 |
|---|---|
| Proprietary name | calcipotriene and betamethasone dipropionate |
| Nonproprietary name | calcipotriene and betamethasone dipropionate |
| Substances | BETAMETHASONE DIPROPIONATE, CALCIPOTRIENE |
| Dosage form | SUSPENSION |
| Route | TOPICAL |
| Labeler | Cosette Pharmaceuticals, Inc. |
| Product type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Application number | ANDA210765 |
| Pharmacologic classes | Corticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC], Vitamin D Analog [EPC], Vitamin D [CS] |
| Marketing start | Aug 2, 2024 |
| Listing certified through | Dec 31, 2026 |
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: