NDC product
PANADOL Extra Strength
NDC 0135-0135 · GlaxoSmithKline Consumer Healthcare Holdings (US) LLC
Key facts
| Product NDC | 0135-0135 |
|---|---|
| Proprietary name | PANADOL |
| Labeler | GlaxoSmithKline Consumer Healthcare Holdings (US) LLC |
| Marketing category | OTC MONOGRAPH NOT FINAL |
| Application number | part343 |
| Marketing start | Mar 18, 2011 |
| Marketing end | Nov 30, 2018 |
| Listing certified through | Nov 30, 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: