FDA NDC Directory · JSON-LD · Markdown

Divalproex sodium

NDC 0615-8237 · HUMAN PRESCRIPTION DRUG · CAPSULE

Labeler / ManufacturerNCS HealthCare of KY, LLC dba Vangard Labs
Marketing categoryAbbreviated NDA (generic) · App ANDA078979
Dosage form / routeCAPSULE · ORAL
Active ingredientsDIVALPROEX SODIUM (125 mg/1)
Marketing started20090123
Package count4

External sources

Source: openFDA. Public-domain (CC0).