NDC product
TUMS ULTRA
NDC 0135-0182 · GlaxoSmithKline Consumer Heathcare LP
Key facts
| Product NDC | 0135-0182 |
|---|---|
| Proprietary name | TUMS |
| Labeler | GlaxoSmithKline Consumer Heathcare LP |
| Marketing category | OTC MONOGRAPH FINAL |
| Application number | part331 |
| Marketing start | Feb 12, 2010 |
| Marketing end | Nov 18, 2011 |
| Listing certified through | Nov 18, 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: