NDC 83723-010 – Sofdra

Sofpironium Bromide 87 mg/.67mL · Gel · Topical

Human Prescription Drug

Product NDC83723-010

Product details

Brand name
Sofdra
Generic name
sofpironium bromide
Labeler
Botanix SB Inc.
Dosage form
Gel
Route
Topical
Marketing category
NDA · NDA217347
Marketed since
August 6, 2024
Listing expires
December 31, 2026

Active ingredients

Uses, dosage, side effects and warnings for Sofdra →

Package NDC codes (1)

Package NDCDescriptionSince
83723-010-501 BOTTLE in 1 CARTON (83723-010-50) / 50 mL in 1 BOTTLEAug 6, 2024