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LURASIDONE HYDROCHLORIDE

NDC 65862-956 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerAurobindo Pharma Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA208045
Dosage form / routeTABLET · ORAL
Active ingredientsLURASIDONE HYDROCHLORIDE (80 mg/1)
Marketing started20230310
Package count3

External sources

Source: openFDA. Public-domain (CC0).