FDA NDC Directory · JSON-LD · Markdown

tadalafil

NDC 76420-855 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerAsclemed USA, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA209250
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsTADALAFIL (5 mg/1)
Marketing started20190326
Package count6

External sources

Source: openFDA. Public-domain (CC0).