FDA NDC Directory · JSON-LD · Markdown

Tadalafil

NDC 82804-040 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerProficient Rx LP
Marketing categoryAbbreviated NDA (generic) · App ANDA211298
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsTADALAFIL (5 mg/1)
Marketing started20201102
Package count3

External sources

Source: openFDA. Public-domain (CC0).