DIVALPROEX SODIUM
Summary
FDA approved DIVALPROEX SODIUM by AJANTA PHARMA LTD. ANDA (Generic) approval (Labeling) on 2024-07-15. CAPSULE, DELAYED REL PELLETS, ORAL.
Details
Source
Drug Approval
External ID
ANDA213181-18
Action Date
2024-07-15
Status
Approved
Category
drug
Product Code
ANDA (Generic)
Product Description
DIVALPROEX SODIUM, CAPSULE, DELAYED REL PELLETS, ORAL. Application: ANDA213181
Company
Context & Analysis
AJANTA PHARMA LTD has 26 FDA actions in our database, including 3 recalls.
Frequently Asked Questions
How often does AJANTA PHARMA LTD have FDA actions?
AJANTA PHARMA LTD has 26 FDA actions in our database, including 3 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "ANDA213181-18" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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