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Depakote

NDC 0074-7326 · HUMAN PRESCRIPTION DRUG · TABLET, DELAYED RELEASE

Generic nameDivalproex Sodium
Labeler / ManufacturerAbbVie Inc.
Marketing categoryNew Drug Application (innovator) · App NDA018723
Dosage form / routeTABLET, DELAYED RELEASE · ORAL
Active ingredientsDIVALPROEX SODIUM (250 mg/1)
Marketing started20230630
Package count1

External sources

Source: openFDA. Public-domain (CC0).