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Lurasidone hydrochloride

NDC 70771-1735 · HUMAN PRESCRIPTION DRUG · TABLET, COATED

Labeler / ManufacturerZydus Lifesciences Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA208052
Dosage form / routeTABLET, COATED · ORAL
Active ingredientsLURASIDONE HYDROCHLORIDE (40 mg/1)
Marketing started20230201
Package count5

External sources

Source: openFDA. Public-domain (CC0).