FDA NDC Directory · JSON-LD · Markdown

Tadalafil

NDC 71205-720 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerProficient Rx LP
Marketing categoryAbbreviated NDA (generic) · App ANDA209167
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsTADALAFIL (10 mg/1)
Marketing started20200403
Package count1

External sources

Source: openFDA. Public-domain (CC0).