FDA NDC Directory · JSON-LD · Markdown

DIVALPROEX SODIUM

NDC 61919-249 · HUMAN PRESCRIPTION DRUG · TABLET, DELAYED RELEASE

Generic namedivalproex sodium
Labeler / ManufacturerDirectRx
Marketing categoryAbbreviated NDA (generic) · App ANDA079163
Dosage form / routeTABLET, DELAYED RELEASE · ORAL
Active ingredientsDIVALPROEX SODIUM (500 mg/1)
Marketing started20220406
Package count2

External sources

Source: openFDA. Public-domain (CC0).