FDA NDC Directory · JSON-LD · Markdown

TICAGRELOR

NDC 43547-657 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Generic nameticagrelor
Labeler / ManufacturerSolco Healthcare U.S., LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA208599
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsTICAGRELOR (90 mg/1)
Marketing started20250401
Package count3

External sources

Source: openFDA. Public-domain (CC0).