FDA NDC Directory · JSON-LD · Markdown

Tadalafil

NDC 80425-0443 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerAdvanced Rx of Tennessee, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA210420
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsTADALAFIL (20 mg/1)
Marketing started20241015
Package count1

External sources

Source: openFDA. Public-domain (CC0).