NDC product
Divalproex Sodium
NDC 0115-6922 · Amneal Pharmaceuticals of New York LLC
Key facts
| Product NDC | 0115-6922 |
|---|---|
| Proprietary name | Divalproex Sodium |
| Labeler | Amneal Pharmaceuticals of New York LLC |
| Marketing category | ANDA |
| Application number | ANDA078791 |
| Marketing start | Aug 4, 2009 |
| Marketing end | Oct 31, 2019 |
| Listing certified through | Oct 31, 2019 |
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: