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Lurasidone Hydrochloride

NDC 53746-082 · HUMAN PRESCRIPTION DRUG · TABLET, COATED

Labeler / ManufacturerAmneal Pharmaceuticals of New York LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA208002
Dosage form / routeTABLET, COATED · ORAL
Active ingredientsLURASIDONE HYDROCHLORIDE (60 mg/1)
Marketing started20240705
Package count1

External sources

Source: openFDA. Public-domain (CC0).