NDC product
Atazanavir Sulfate
NDC 0093-5527 · Teva Pharmaceuticals USA, Inc.
Key facts
| Product NDC | 0093-5527 |
|---|---|
| Proprietary name | Atazanavir Sulfate |
| Nonproprietary name | Atazanavir Sulfate |
| Substances | ATAZANAVIR SULFATE |
| Dosage form | CAPSULE |
| Route | ORAL |
| Labeler | Teva Pharmaceuticals USA, Inc. |
| Product type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Application number | ANDA091673 |
| Pharmacologic classes | Cytochrome P450 2C8 Inhibitors [MoA], Cytochrome P450 3A Inhibitors [MoA], Cytochrome P450 3A4 Inhibitors [MoA], HIV Protease Inhibitors [MoA], Protease Inhibitor [EPC], UDP Glucuronosyltransferases Inhibitors [MoA] and 1 more |
| Marketing start | Dec 27, 2017 |
| Listing certified through | Dec 31, 2026 |
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: