NDC product
Norditropin
NDC 0169-7770 · Novo Nordisk
Key facts
| Product NDC | 0169-7770 |
|---|---|
| Proprietary name | Norditropin |
| Labeler | Novo Nordisk |
| Marketing category | NDA |
| Application number | NDA021148 |
| Marketing start | Oct 2, 2000 |
| Marketing end | Nov 14, 2012 |
| Listing certified through | Nov 14, 2012 |
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: