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Ticagrelor

NDC 42658-115 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerHisun Pharmaceuticals USA, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA208575
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsTICAGRELOR (90 mg/1)
Marketing started20250501
Package count1

External sources

Source: openFDA. Public-domain (CC0).