FDA NDC Directory · JSON-LD · Markdown

Tadalafil

NDC 71610-567 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerAphena Pharma Solutions - Tennessee, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA209744
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsTADALAFIL (20 mg/1)
Marketing started20210121
Package count4

External sources

Source: openFDA. Public-domain (CC0).