NDC product
Fosinopril sodium
NDC 24658-100 · Blu Pharmaceuticals, LLC
Key facts
| Product NDC | 24658-100 |
|---|---|
| Proprietary name | Fosinopril sodium |
| Labeler | Blu Pharmaceuticals, LLC |
| Marketing category | ANDA |
| Application number | ANDA077222 |
| Marketing start | Sep 22, 2006 |
| Marketing end | Aug 28, 2007 |
| Listing certified through | Aug 28, 2007 |
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: