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Divalproex Sodium

NDC 68071-3553 · HUMAN PRESCRIPTION DRUG · TABLET, DELAYED RELEASE

Labeler / ManufacturerNuCare Pharmaceuticals,Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA078597
Dosage form / routeTABLET, DELAYED RELEASE · ORAL
Active ingredientsDIVALPROEX SODIUM (250 mg/1)
Marketing started20080729
Package count1

External sources

Source: openFDA. Public-domain (CC0).