FDA NDC Directory · JSON-LD · Markdown

tadalafil

NDC 71821-009 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Generic nameTadalafil
Labeler / ManufacturerVKT Pharma Private Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA215556
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsTADALAFIL (20 mg/1)
Marketing started20211104
Package count1

External sources

Source: openFDA. Public-domain (CC0).