FDA NDC Directory · JSON-LD · Markdown

Eulexin

NDC 80725-143 · HUMAN PRESCRIPTION DRUG · CAPSULE

Generic nameFlutamide
Labeler / ManufacturerWaylis Therapeutics LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA075298
Dosage form / routeCAPSULE · ORAL
Active ingredientsFLUTAMIDE (125 mg/1)
Marketing started20211112
Package count1

External sources

Source: openFDA. Public-domain (CC0).