DIVALPROEX SODIUM (DIVALPROEX SODIUM) — FDA Approval ANDA213181 (AJANTA PHARMA LTD)
DIVALPROEX SODIUM (DIVALPROEX SODIUM) — FDA Approval ANDA213181 (AJANTA PHARMA LTD) is one of 9,000 drug approvals in the DrugApprovals dataset. Key details — Brand name: DIVALPROEX SODIUM; Active ingredients: DIVALPROEX SODIUM; Application number: ANDA213181.
| Brand name | DIVALPROEX SODIUM |
|---|---|
| Active ingredients | DIVALPROEX SODIUM |
| Application number | ANDA213181 |
| Sponsor | AJANTA PHARMA LTD |
| Dosage form | CAPSULE, DELAYED REL PELLETS |
| Route | ORAL |
| Marketing status | Prescription |
| Products in application | 1 |
| First approval date | 20200228 |
| Source | openFDA Drugs@FDA |
$1499/mo
Try DrugApprovals →