NDC product
Divalproex Sodium Delayed-Release
NDC 0603-3442 · Qualitest Pharmaceuticals
Key facts
| Product NDC | 0603-3442 |
|---|---|
| Proprietary name | Divalproex Sodium |
| Labeler | Qualitest Pharmaceuticals |
| Marketing category | ANDA |
| Application number | ANDA090210 |
| Marketing start | Nov 30, 2009 |
| Marketing end | May 27, 2012 |
| Listing certified through | May 27, 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: