NDC product
Cetirizine Hydrochloride
NDC 0121-4780 · PAI Holdings, LLC
Key facts
| Product NDC | 0121-4780 |
|---|---|
| Proprietary name | Cetirizine Hydrochloride |
| Labeler | PAI Holdings, LLC |
| Marketing category | ANDA |
| Application number | ANDA090300 |
| Marketing start | Sep 15, 2009 |
| Marketing end | Aug 30, 2013 |
| Listing certified through | Aug 30, 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: