FDA NDC Directory · JSON-LD · Markdown

Armodafinil

NDC 65862-998 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerAurobindo Pharma Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA206069
Dosage form / routeTABLET · ORAL
Active ingredientsARMODAFINIL (200 mg/1)
Marketing started20181207
Package count1

External sources

Source: openFDA. Public-domain (CC0).