NDC product
Hydroxychloroquine Sulfate
NDC 0093-2401 · Teva Pharmaceuticals USA, Inc.
Key facts
| Product NDC | 0093-2401 |
|---|---|
| Proprietary name | Hydroxychloroquine Sulfate |
| Nonproprietary name | Hydroxychloroquine Sulfate |
| Substances | HYDROXYCHLOROQUINE SULFATE |
| Dosage form | TABLET, FILM COATED |
| Route | ORAL |
| Labeler | Teva Pharmaceuticals USA, Inc. |
| Product type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Application number | ANDA040081 |
| Pharmacologic classes | Antimalarial [EPC], Antirheumatic Agent [EPC] |
| Marketing start | Oct 8, 2020 |
| Marketing end | Nov 30, 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