FDA NDC Directory · JSON-LD · Markdown

ADCIRCA

NDC 66302-467 · HUMAN PRESCRIPTION DRUG · TABLET

Generic nameTadalafil
Labeler / ManufacturerUnited Therapeutics Corporation
Marketing categoryNew Drug Application (innovator) · App NDA022332
Dosage form / routeTABLET · ORAL
Active ingredientsTADALAFIL (20 mg/1)
Marketing started20090522
Package count1

External sources

Source: openFDA. Public-domain (CC0).