FDA NDC Directory · JSON-LD · Markdown

Modafinil

NDC 57237-155 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerRising Pharma Holdings, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA202566
Dosage form / routeTABLET · ORAL
Active ingredientsMODAFINIL (200 mg/1)
Marketing started20120927
Package count3

External sources

Source: openFDA. Public-domain (CC0).