FDA NDC Directory · JSON-LD · Markdown

Modafinil

NDC 72578-006 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerViona Pharmaceuticals Inc
Marketing categoryAbbreviated NDA (generic) · App ANDA209966
Dosage form / routeTABLET · ORAL
Active ingredientsMODAFINIL (200 mg/1)
Marketing started20190215
Package count3

External sources

Source: openFDA. Public-domain (CC0).