NDC 85437-093 – Auranofin

Auranofin 3 mg/1 · Capsule · Oral

Human Prescription Drug

Product NDC85437-093

Product details

Brand name
Auranofin
Generic name
auranofin
Labeler
Coral Way Pharma, LLC
Dosage form
Capsule
Route
Oral
Marketing category
NDA AUTHORIZED GENERIC · NDA018689
Marketed since
October 29, 2025
Listing expires
December 31, 2026

Active ingredients

Uses, dosage, side effects and warnings for Auranofin →

Package NDC codes (1)

Package NDCDescriptionSince
85437-093-0660 CAPSULE in 1 BOTTLE (85437-093-06)Oct 29, 2025