NDC product
Fexofenadine Hydrochloride
NDC 0555-0721 · Barr Laboratories Inc.
Key facts
| Product NDC | 0555-0721 |
|---|---|
| Proprietary name | Fexofenadine Hydrochloride |
| Labeler | Barr Laboratories Inc. |
| Marketing category | ANDA |
| Application number | ANDA076191 |
| Marketing start | Nov 17, 2006 |
| Marketing end | May 22, 2012 |
| Listing certified through | May 22, 2012 |
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: