FDA NDC Directory · JSON-LD · Markdown

Tadalafil

NDC 76420-642 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerAsclemed USA, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA207244
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsTADALAFIL (5 mg/1)
Marketing started20191008
Package count3

External sources

Source: openFDA. Public-domain (CC0).