FDA NDC Directory · JSON-LD · Markdown

Divalproex Sodium ER

NDC 72189-459 · HUMAN PRESCRIPTION DRUG · TABLET, EXTENDED RELEASE

Labeler / ManufacturerDirect_Rx
Marketing categoryAbbreviated NDA (generic) · App ANDA209286
Dosage form / routeTABLET, EXTENDED RELEASE · ORAL
Active ingredientsDIVALPROEX SODIUM (500 mg/1)
Marketing started20230403
Package count1

External sources

Source: openFDA. Public-domain (CC0).