NDC product
TEMOVATE E
NDC 10337-301 · Fougera Pharmaceuticals Inc.
Key facts
| Product NDC | 10337-301 |
|---|---|
| Proprietary name | TEMOVATE E |
| Labeler | Fougera Pharmaceuticals Inc. |
| Marketing category | ANDA |
| Application number | ANDA075430 |
| Marketing start | May 26, 1999 |
| Marketing end | May 26, 1999 |
| Listing certified through | May 26, 1999 |
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: