NDC 0299-3823 – Soolantra

Ivermectin 10 mg/g · Cream · Topical

Human Prescription Drug

Product NDC0299-3823

Product details

Brand name
Soolantra
Generic name
Ivermectin
Labeler
Galderma Laboratories, L.P.
Dosage form
Cream
Route
Topical
Marketing category
NDA · NDA206255
Marketed since
January 1, 2015
Listing expires
December 31, 2026
Pharmacologic class
Antiparasitic; Pediculicide

Active ingredients

Uses, dosage, side effects and warnings for Soolantra →

Package NDC codes (5)

Package NDCDescriptionSince
0299-3823-00 sample2 g in 1 TUBE (0299-3823-00)Nov 1, 2019
0299-3823-02 sample1 TUBE in 1 BLISTER PACK (0299-3823-02) / 2 g in 1 TUBEJan 1, 2015
0299-3823-301 TUBE in 1 CARTON (0299-3823-30) / 30 g in 1 TUBEJan 1, 2015
0299-3823-451 TUBE in 1 CARTON (0299-3823-45) / 45 g in 1 TUBEJan 1, 2015
0299-3823-601 TUBE in 1 CARTON (0299-3823-60) / 60 g in 1 TUBEJan 1, 2015