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Divalproex sodium

NDC 16714-484 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED, EXTENDED RELEASE

Labeler / ManufacturerNorthStar Rx LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA202419
Dosage form / routeTABLET, FILM COATED, EXTENDED RELEASE · ORAL
Active ingredientsDIVALPROEX SODIUM (250 mg/1)
Marketing started20140602
Package count2

External sources

Source: openFDA. Public-domain (CC0).