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lurasidone hydrochloride

NDC 72603-622 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerNorthStar RxLLC
Marketing categoryAbbreviated NDA (generic) · App ANDA212124
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsLURASIDONE HYDROCHLORIDE (40 mg/1)
Marketing started20250408
Package count1

External sources

Source: openFDA. Public-domain (CC0).