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Divalproex Sodium

NDC 55111-534 · HUMAN PRESCRIPTION DRUG · TABLET, EXTENDED RELEASE

Labeler / ManufacturerDr. Reddy's Laboratories Ltd
Marketing categoryAbbreviated NDA (generic) · App ANDA090070
Dosage form / routeTABLET, EXTENDED RELEASE · ORAL
Active ingredientsDIVALPROEX SODIUM (500 mg/1)
Marketing started20130811
Package count4

External sources

Source: openFDA. Public-domain (CC0).