DEPAKOTE (DIVALPROEX SODIUM)
Summary
FDA approved DEPAKOTE (DIVALPROEX SODIUM) by ABBVIE. NDA (New Drug) approval (Labeling) on 2026-03-31. TABLET, DELAYED RELEASE, ORAL.
Details
Source
Drug Approval
External ID
NDA018723-73
Action Date
2026-03-31
Status
Approved
Category
drug
Product Code
NDA (New Drug)
Product Description
DEPAKOTE (generic: DIVALPROEX SODIUM), TABLET, DELAYED RELEASE, ORAL. Application: NDA018723
Company
Context & Analysis
ABBVIE has 29 FDA actions in our database.
Frequently Asked Questions
How often does ABBVIE have FDA actions?
ABBVIE has 29 FDA actions in our database, including 0 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "NDA018723-73" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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