NDC product
Deferasirox
NDC 0480-7013 · Teva Pharmaceuticals, Inc.
Key facts
| Product NDC | 0480-7013 |
|---|---|
| Proprietary name | Deferasirox |
| Nonproprietary name | Deferasirox |
| Substances | DEFERASIROX |
| Dosage form | TABLET, FOR SUSPENSION |
| Route | ORAL |
| Labeler | Teva Pharmaceuticals, Inc. |
| Product type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Application number | ANDA207124 |
| Pharmacologic classes | Cytochrome P450 1A2 Inhibitors [MoA], Cytochrome P450 2C8 Inhibitors [MoA], Cytochrome P450 3A4 Inducers [MoA], Iron Chelating Activity [MoA], Iron Chelator [EPC] |
| Marketing start | Nov 1, 2024 |
| Listing certified through | Dec 31, 2027 |
At a glance
- 1–9 Package NDCs
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
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: