FDA NDC Directory · JSON-LD · Markdown

divalproex sodium

NDC 17856-0109 · HUMAN PRESCRIPTION DRUG · CAPSULE, COATED PELLETS

Labeler / ManufacturerATLANTIC BIOLOGICALS CORP.
Marketing categoryAbbreviated NDA (generic) · App ANDA078919
Dosage form / routeCAPSULE, COATED PELLETS · ORAL
Active ingredientsDIVALPROEX SODIUM (125 mg/1)
Marketing started20190131
Package count1

External sources

Source: openFDA. Public-domain (CC0).