NDC product
Divalproex Sodium
NDC 0832-7123 · Upsher-Smith Laboratories, LLC
Key facts
| Product NDC | 0832-7123 |
|---|---|
| Proprietary name | Divalproex Sodium |
| Nonproprietary name | Divalproex Sodium |
| Substances | DIVALPROEX SODIUM |
| Dosage form | TABLET, DELAYED RELEASE |
| Route | ORAL |
| Labeler | Upsher-Smith Laboratories, LLC |
| Product type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Application number | ANDA078182 |
| Pharmacologic classes | Anti-epileptic Agent [EPC], Decreased Central Nervous System Disorganized Electrical Activity [PE], Mood Stabilizer [EPC] |
| Marketing start | Mar 21, 2014 |
| Marketing end | Oct 31, 2027 |
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