NDC product
TALWIN Nx
NDC 0024-1951 · sanofi-aventis U.S. LLC
Key facts
| Product NDC | 0024-1951 |
|---|---|
| Proprietary name | TALWIN Nx |
| Labeler | sanofi-aventis U.S. LLC |
| Marketing category | NDA |
| Application number | NDA018733 |
| Marketing start | Sep 23, 1982 |
| Marketing end | Apr 29, 2002 |
| Listing certified through | Apr 29, 2002 |
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: