NDC product
Valproic Acid
NDC 0832-1008 · Upsher-Smith Laboratories, Inc
Key facts
| Product NDC | 0832-1008 |
|---|---|
| Proprietary name | Valproic Acid |
| Labeler | Upsher-Smith Laboratories, Inc |
| Marketing category | ANDA |
| Application number | ANDA073229 |
| Marketing start | Oct 29, 1991 |
| Marketing end | Dec 30, 2005 |
| Listing certified through | Dec 30, 2005 |
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: