FDA NDC Directory · JSON-LD · Markdown

PITOLISANT

NDC 70748-387 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Generic namepitolisant
Labeler / ManufacturerLupin Pharmaceuticals, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA218846
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsPITOLISANT HYDROCHLORIDE (17.8 mg/1)
Marketing started20261016
Package count1

External sources

Source: openFDA. Public-domain (CC0).