FDA NDC Directory · JSON-LD · Markdown

TADALAFIL

NDC 68071-3753 · HUMAN PRESCRIPTION DRUG · TABLET

Generic nametadalafil
Labeler / ManufacturerNuCare Pharmaceuticals,Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA210609
Dosage form / routeTABLET · ORAL
Active ingredientsTADALAFIL (20 mg/1)
Marketing started20220118
Package count1

External sources

Source: openFDA. Public-domain (CC0).