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Lurasidone Hydrochloride

NDC 47335-684 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerSun Pharmaceutical Industries, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA208066
Dosage form / routeTABLET · ORAL
Active ingredientsLURASIDONE HYDROCHLORIDE (40 mg/1)
Marketing started20230220
Package count3

External sources

Source: openFDA. Public-domain (CC0).