DIVALPROEX SODIUM (DIVALPROEX SODIUM) — FDA Approval ANDA077615 (APOTEX)
DIVALPROEX SODIUM (DIVALPROEX SODIUM) — FDA Approval ANDA077615 (APOTEX) is one of 9,000 drug approvals in the DrugApprovals dataset. Key details — Brand name: DIVALPROEX SODIUM; Active ingredients: DIVALPROEX SODIUM; Application number: ANDA077615.
| Brand name | DIVALPROEX SODIUM |
|---|---|
| Active ingredients | DIVALPROEX SODIUM |
| Application number | ANDA077615 |
| Sponsor | APOTEX |
| Dosage form | TABLET, DELAYED RELEASE |
| Route | ORAL |
| Marketing status | Discontinued |
| Products in application | 3 |
| First approval date | 20080729 |
| Source | openFDA Drugs@FDA |
$1499/mo
Try DrugApprovals →