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Lurasidone Hydrochloride

NDC 23155-889 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerHeritage Pharma Labs Inc. d/b/a Avet Pharmaceuticals Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA208058
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsLURASIDONE HYDROCHLORIDE (60 mg/1)
Marketing started20231019
Package count4

External sources

Source: openFDA. Public-domain (CC0).