NDC product
Prazosin Hydrochloride
NDC 24236-861 · REMEDYREPACK INC.
Key facts
| Product NDC | 24236-861 |
|---|---|
| Proprietary name | Prazosin Hydrochloride |
| Labeler | REMEDYREPACK INC. |
| Marketing category | ANDA |
| Application number | ANDA072575 |
| Marketing start | Oct 20, 2008 |
| Marketing end | Aug 13, 2018 |
| Listing certified through | Aug 13, 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: