NDC product
Oxandrolone
NDC 0245-0271 · Upsher-Smith Laboratories, LLC
Key facts
| Product NDC | 0245-0271 |
|---|---|
| Proprietary name | Oxandrolone |
| Labeler | Upsher-Smith Laboratories, LLC |
| Marketing category | ANDA |
| Application number | ANDA076761 |
| Marketing start | Dec 1, 2006 |
| Marketing end | Mar 14, 2024 |
| Listing certified through | Mar 14, 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: