NDC product
Fexofenadine Hydrochloride
NDC 0480-7253 · Teva Pharmaceutical Industries Ltd.
Key facts
| Product NDC | 0480-7253 |
|---|---|
| Proprietary name | Fexofenadine Hydrochloride |
| Labeler | Teva Pharmaceutical Industries Ltd. |
| Marketing category | ANDA |
| Application number | ANDA076447 |
| Marketing start | Sep 17, 2010 |
| Marketing end | Dec 26, 2013 |
| Listing certified through | Dec 26, 2013 |
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: