FDA NDC Directory · JSON-LD · Markdown

TADALAFIL

NDC 70518-3931 · HUMAN PRESCRIPTION DRUG · TABLET

Generic nametadalafil
Labeler / ManufacturerREMEDYREPACK INC.
Marketing categoryAbbreviated NDA (generic) · App ANDA210608
Dosage form / routeTABLET · ORAL
Active ingredientsTADALAFIL (20 mg/1)
Marketing started20231204
Package count2

External sources

Source: openFDA. Public-domain (CC0).