NDC product
REPREXAIN
NDC 23710-900 · Quinnova Pharmaceuticals, LLC
Key facts
| Product NDC | 23710-900 |
|---|---|
| Proprietary name | REPREXAIN |
| Labeler | Quinnova Pharmaceuticals, LLC |
| Marketing category | ANDA |
| Application number | ANDA076642 |
| Marketing start | Feb 18, 2010 |
| Marketing end | Aug 30, 2012 |
| Listing certified through | Aug 30, 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: