NDC product
Oxaliplatin
NDC 0517-1910 · American Regent, Inc.
Key facts
| Product NDC | 0517-1910 |
|---|---|
| Proprietary name | Oxaliplatin |
| Labeler | American Regent, Inc. |
| Marketing category | ANDA |
| Application number | ANDA204378 |
| Marketing start | Dec 12, 2017 |
| Marketing end | Dec 12, 2017 |
| Listing certified through | Dec 12, 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: