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divalproex sodium

NDC 0615-8586 · HUMAN PRESCRIPTION DRUG · TABLET, DELAYED RELEASE

Labeler / ManufacturerNCS HealthCare of KY, LLC dba Vangard Labs
Marketing categoryAbbreviated NDA (generic) · App ANDA078853
Dosage form / routeTABLET, DELAYED RELEASE · ORAL
Active ingredientsDIVALPROEX SODIUM (125 mg/1)
Marketing started20240626
Package count1

External sources

Source: openFDA. Public-domain (CC0).