FDA NDC Directory · JSON-LD · Markdown

Divalproex Sodium

NDC 68084-313 · HUMAN PRESCRIPTION DRUG · CAPSULE, COATED PELLETS

Labeler / ManufacturerAmerican Health Packaging
Marketing categoryAbbreviated NDA (generic) · App ANDA078919
Dosage form / routeCAPSULE, COATED PELLETS · ORAL
Active ingredientsDIVALPROEX SODIUM (125 mg/1)
Marketing started20090318
Package count2

External sources

Source: openFDA. Public-domain (CC0).