FDA NDC Directory · JSON-LD · Markdown

Modafinil

NDC 60505-2526 · HUMAN PRESCRIPTION DRUG · TABLET

Generic namemodafinil
Labeler / ManufacturerApotex Corp.
Marketing categoryAbbreviated NDA (generic) · App ANDA077667
Dosage form / routeTABLET · ORAL
Active ingredientsMODAFINIL (100 mg/1)
Marketing started20140203
Package count2

External sources

Source: openFDA. Public-domain (CC0).