NDC product
ROBITUSSIN PEAK COLD DAYTIME COLD PLUS FLU
NDC 0031-8721 · GlaxoSmithKline Consumer Healthcare Holdings (US) LLC
Key facts
| Product NDC | 0031-8721 |
|---|---|
| Proprietary name | ROBITUSSIN PEAK COLD DAYTIME COLD PLUS FLU |
| Labeler | GlaxoSmithKline Consumer Healthcare Holdings (US) LLC |
| Marketing category | UNAPPROVED DRUG OTHER |
| Marketing start | Apr 15, 2012 |
| Marketing end | Jun 30, 2017 |
| Listing certified through | Jun 30, 2017 |
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: