FDA NDC Directory · JSON-LD · Markdown

Tadalafil

NDC 68071-2553 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerNuCare Pharmaceuticals,Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA209167
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsTADALAFIL (20 mg/1)
Marketing started20190327
Package count1

External sources

Source: openFDA. Public-domain (CC0).