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Lurasidone Hydrochloride

NDC 13668-737 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerTorrent Pharmaceuticals Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA208055
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsLURASIDONE HYDROCHLORIDE (60 mg/1)
Marketing started20260302
Package count2

External sources

Source: openFDA. Public-domain (CC0).