FDA NDC Directory · JSON-LD · Markdown

VALPROIC ACID

NDC 0121-1350 · HUMAN PRESCRIPTION DRUG · SOLUTION

Labeler / ManufacturerPAI Holdings, LLC dba PAI Pharma
Marketing categoryAbbreviated NDA (generic) · App ANDA075379
Dosage form / routeSOLUTION · ORAL
Active ingredientsVALPROIC ACID (500 mg/10mL)
Marketing started20050411
Package count1

External sources

Source: openFDA. Public-domain (CC0).