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Lurasidone hydrochloride

NDC 70518-4117 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerREMEDYREPACK INC.
Marketing categoryAbbreviated NDA (generic) · App ANDA208047
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsLURASIDONE HYDROCHLORIDE (40 mg/1)
Marketing started20240627
Package count2

External sources

Source: openFDA. Public-domain (CC0).