NDC product
fexofenadine hydrochloride
NDC 21130-571 · Safeway
Key facts
| Product NDC | 21130-571 |
|---|---|
| Proprietary name | fexofenadine hydrochloride |
| Labeler | Safeway |
| Marketing category | ANDA |
| Application number | ANDA076447 |
| Marketing start | Apr 15, 2011 |
| Marketing end | Dec 24, 2014 |
| Listing certified through | Dec 24, 2014 |
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: