NDC product
Oxycodone Hydrochloride
NDC 0054-0522 · West-Ward Pharmaceuticals Corp.
Key facts
| Product NDC | 0054-0522 |
|---|---|
| Proprietary name | Oxycodone Hydrochloride |
| Labeler | West-Ward Pharmaceuticals Corp. |
| Marketing category | ANDA |
| Application number | ANDA203208 |
| Marketing start | Jul 16, 2013 |
| Marketing end | Sep 11, 2017 |
| Listing certified through | Sep 11, 2017 |
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: