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divalproex sodium

NDC 68001-647 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED, EXTENDED RELEASE

Labeler / ManufacturerBluePoint Laboratories
Marketing categoryAbbreviated NDA (generic) · App ANDA214643
Dosage form / routeTABLET, FILM COATED, EXTENDED RELEASE · ORAL
Active ingredientsDIVALPROEX SODIUM (500 mg/1)
Marketing started20250606
Package count2

External sources

Source: openFDA. Public-domain (CC0).