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Armodafinil

NDC 69339-178 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerNatco Pharma USA LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA202768
Dosage form / routeTABLET · ORAL
Active ingredientsARMODAFINIL (150 mg/1)
Marketing started20230323
Package count2

External sources

Source: openFDA. Public-domain (CC0).