NDC product
Hydroxyzine Hydrochloride
NDC 0121-4822 · Pharmaceutical Associates, Inc.
Key facts
| Product NDC | 0121-4822 |
|---|---|
| Proprietary name | Hydroxyzine Hydrochloride |
| Labeler | Pharmaceutical Associates, Inc. |
| Marketing category | ANDA |
| Application number | ANDA087294 |
| Marketing start | Jan 1, 2015 |
| Marketing end | Jul 31, 2018 |
| Listing certified through | Jul 31, 2018 |
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: