FDA NDC Directory · JSON-LD · Markdown

Latuda

NDC 63402-308 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Generic namelurasidone hydrochloride
Labeler / ManufacturerSumitomo Pharma America, Inc.
Marketing categoryNew Drug Application (innovator) · App NDA200603
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsLURASIDONE HYDROCHLORIDE (80 mg/1)
Marketing started20101028
Package count5

External sources

Source: openFDA. Public-domain (CC0).