FDA NDC Directory · JSON-LD · Markdown

TADALAFIL

NDC 72303-0824 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Generic nameTadalafil
Labeler / ManufacturerHEC Pharm USA Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA211335
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsTADALAFIL (10 mg/1)
Marketing started20190327
Package count1

External sources

Source: openFDA. Public-domain (CC0).