FDA NDC Directory · JSON-LD · Markdown

Tadalafil

NDC 16714-075 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerNorthStar RxLLC
Marketing categoryAbbreviated NDA (generic) · App ANDA208934
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsTADALAFIL (5 mg/1)
Marketing started20200219
Package count1

External sources

Source: openFDA. Public-domain (CC0).