Drug application
DEPAKOTE CP (DIVALPROEX SODIUM)
Drugs@FDA NDA 019794 · ABBOTT
Key facts
| Drug name | DEPAKOTE CP |
|---|---|
| Active ingredients | DIVALPROEX SODIUM |
| Application type | NDA |
| Application number | 019794 |
| Company | ABBOTT |
| Dosage forms | TABLET, DELAYED RELEASE, ORAL |
| Strength | EQ 250MG BASE |
| Marketing status | Discontinued |
| Reference listed drug | No |
| Latest submission class | Type 3 - New Dosage Form |
| Latest submission status date | Jul 11, 1990 |
At a glance
- 1–9 Submissions
- 1–9 Supplements
- None Label versions
- 1–9 Products
- None Therapeutic equivalents
- No FDA letters on file
- No FDA reviews on file
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About Drugs@FDA applications
Drugs@FDA covers FDA-approved brand-name and generic drugs and therapeutic biologics, with their applications (NDA, ANDA or BLA), products, submissions and labels.
Source: U.S. Food and Drug Administration (FDA), Drugs@FDA · Source date: