FDA NDC Directory · JSON-LD · Markdown

PERAMPANEL

NDC 51672-4256 · HUMAN PRESCRIPTION DRUG · SUSPENSION

Labeler / ManufacturerSun Pharmaceutical Industries, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA219052
Dosage form / routeSUSPENSION · ORAL
Active ingredientsPERAMPANEL (.5 mg/mL)
Marketing started20260616
Package count1

External sources

Source: openFDA. Public-domain (CC0).