NDC product
NICORETTE
NDC 0135-0513 · GlaxoSmithKline Consumer Healthcare Holdings (US) LLC
Key facts
| Product NDC | 0135-0513 |
|---|---|
| Proprietary name | NICORETTE |
| Labeler | GlaxoSmithKline Consumer Healthcare Holdings (US) LLC |
| Marketing category | NDA |
| Application number | NDA021330 |
| Marketing start | Oct 19, 2010 |
| Marketing end | Nov 19, 2018 |
| Listing certified through | Nov 19, 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: