FDA NDC Directory · JSON-LD · Markdown

Divalproex Sodium

NDC 17856-0797 · HUMAN PRESCRIPTION DRUG · TABLET, DELAYED RELEASE

Labeler / ManufacturerATLANTIC BIOLOGICALS CORP.
Marketing categoryAbbreviated NDA (generic) · App ANDA078597
Dosage form / routeTABLET, DELAYED RELEASE · ORAL
Active ingredientsDIVALPROEX SODIUM (250 mg/1)
Marketing started20080729
Package count1

External sources

Source: openFDA. Public-domain (CC0).