FDA NDC Directory · JSON-LD · Markdown

VALPROIC ACID

NDC 0904-7620 · HUMAN PRESCRIPTION DRUG · SOLUTION

Labeler / ManufacturerMajor Pharmaceuticals
Marketing categoryAbbreviated NDA (generic) · App ANDA075379
Dosage form / routeSOLUTION · ORAL
Active ingredientsVALPROIC ACID (250 mg/5mL)
Marketing started20260803
Package count2

External sources

Source: openFDA. Public-domain (CC0).