FDA NDC Directory · JSON-LD · Markdown

VALPROIC ACID

NDC 70752-202 · HUMAN PRESCRIPTION DRUG · SOLUTION

Labeler / ManufacturerQUAGEN PHARMACEUTICALS LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA090517
Dosage form / routeSOLUTION · ORAL
Active ingredientsVALPROIC ACID (250 mg/5mL)
Marketing started20240415
Package count1

External sources

Source: openFDA. Public-domain (CC0).