FDA NDC Directory · JSON-LD · Markdown

divalproex sodium

NDC 67046-1683 · HUMAN PRESCRIPTION DRUG · TABLET, DELAYED RELEASE

Labeler / ManufacturerCoupler LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA078853
Dosage form / routeTABLET, DELAYED RELEASE · ORAL
Active ingredientsDIVALPROEX SODIUM (250 mg/1)
Marketing started20260706
Package count1

External sources

Source: openFDA. Public-domain (CC0).