FDA NDC Directory · JSON-LD · Markdown

Modafinil

NDC 69452-343 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerBionpharma Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA078963
Dosage form / routeTABLET · ORAL
Active ingredientsMODAFINIL (200 mg/1)
Marketing started20220228
Package count3

External sources

Source: openFDA. Public-domain (CC0).