approval · primary record
DIVALPROEX SODIUM
FDA · NDA · 2026-03-31
| Agency | FDA |
|---|---|
| Submission type | NDA |
| Action date | 2026-03-31 |
| Brand | DEPAKOTE ER |
| Sponsor | ABBVIE |
| Route | ORAL |
Provenance
- Source: openFDA Drugs@FDA
- Fetched at: 2026-10-28T02:34:38.210Z
- Licence class: public-domain
- Verdict: primary-source
- Entity id: FDA:DIVALPROEX SODIUM:2026-03-31
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