NDC product
AUGMENTIN
NDC 0029-6080 · GlaxoSmithKline LLC
Key facts
| Product NDC | 0029-6080 |
|---|---|
| Proprietary name | AUGMENTIN |
| Labeler | GlaxoSmithKline LLC |
| Marketing category | NDA |
| Application number | NDA050564 |
| Marketing start | Oct 22, 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: