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Divalproex Sodium

NDC 48433-034 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED, EXTENDED RELEASE

Generic namedivalproex sodium
Labeler / ManufacturerSafecor Health, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA077567
Dosage form / routeTABLET, FILM COATED, EXTENDED RELEASE · ORAL
Active ingredientsDIVALPROEX SODIUM (500 mg/1)
Marketing started20260224
Package count1

External sources

Source: openFDA. Public-domain (CC0).