FDA NDC Directory · JSON-LD · Markdown

ALYQ

NDC 0480-9277 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Generic nameTadalafil
Labeler / ManufacturerTeva Pharmaceuticals, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA216932
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsTADALAFIL (20 mg/1)
Marketing started20240220
Package count1

External sources

Source: openFDA. Public-domain (CC0).