NDC product
Furosemide
NDC 0517-7502 · American Regent, Inc.
Key facts
| Product NDC | 0517-7502 |
|---|---|
| Proprietary name | Furosemide |
| Labeler | American Regent, Inc. |
| Marketing category | ANDA |
| Application number | ANDA018579 |
| Marketing start | Sep 30, 1990 |
| Marketing end | Sep 2, 2011 |
| Listing certified through | Sep 2, 2011 |
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: