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Modafinil

NDC 70771-1052 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerZydus Lifesciences Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA209966
Dosage form / routeTABLET · ORAL
Active ingredientsMODAFINIL (200 mg/1)
Marketing started20180104
Package count3

External sources

Source: openFDA. Public-domain (CC0).