NDC product
Oxycodone Hydrochloride
NDC 0093-5731 · Teva Pharmaceuticals USA, Inc.
Key facts
| Product NDC | 0093-5731 |
|---|---|
| Proprietary name | Oxycodone Hydrochloride |
| Labeler | Teva Pharmaceuticals USA, Inc. |
| Marketing category | NDA AUTHORIZED GENERIC |
| Application number | NDA022272 |
| Marketing start | Oct 12, 2015 |
| Marketing end | Dec 31, 2024 |
| Listing certified through | Dec 31, 2024 |
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: