FDA NDC Directory · JSON-LD · Markdown

AVODART

NDC 80725-712 · HUMAN PRESCRIPTION DRUG · CAPSULE, LIQUID FILLED

Generic namedutasteride
Labeler / ManufacturerWaylis Therapeutics LLC
Marketing categoryNew Drug Application (innovator) · App NDA021319
Dosage form / routeCAPSULE, LIQUID FILLED · ORAL
Active ingredientsDUTASTERIDE (.5 mg/1)
Marketing started20221215
Package count2

External sources

Source: openFDA. Public-domain (CC0).