FDA NDC Directory · JSON-LD · Markdown

Tadalafil

NDC 60290-030 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerUmedica Laboratories USA Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA211298
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsTADALAFIL (20 mg/1)
Marketing started20260215
Package count5

External sources

Source: openFDA. Public-domain (CC0).