Drug application
DIVALPROEX SODIUM (DIVALPROEX SODIUM)
Drugs@FDA ANDA 217358 · MANKIND PHARMA
Key facts
| Drug name | DIVALPROEX SODIUM |
|---|---|
| Active ingredients | DIVALPROEX SODIUM |
| Application type | ANDA |
| Application number | 217358 |
| Company | MANKIND PHARMA |
| Dosage forms | CAPSULE, DELAYED REL PELLETS, ORAL |
| Strength | EQ 125MG VALPROIC ACID |
| Marketing status | Prescription |
| TE codes | AB |
| Reference listed drug | No |
| Latest submission status date | Aug 12, 2025 |
At a glance
- 1–9 Submissions
- 1–9 Supplements
- None Label versions
- 1–9 Products
- 10–99 Therapeutic equivalents
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.