FDA NDC Directory · JSON-LD · Markdown

lurasidone hydrochloride

NDC 67877-641 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerAscend Laboratories, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA212244
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsLURASIDONE HYDROCHLORIDE (80 mg/1)
Marketing started20230104
Package count4

External sources

Source: openFDA. Public-domain (CC0).