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Divalproex Sodium

NDC 0904-6363 · HUMAN PRESCRIPTION DRUG · TABLET, EXTENDED RELEASE

Labeler / ManufacturerMajor Pharmaceuticals
Marketing categoryAbbreviated NDA (generic) · App ANDA090161
Dosage form / routeTABLET, EXTENDED RELEASE · ORAL
Active ingredientsDIVALPROEX SODIUM (250 mg/1)
Marketing started20130811
Package count2

External sources

Source: openFDA. Public-domain (CC0).