NDC 51672-1395 – Tretinoin

Tretinoin 1 mg/g · Cream · Topical

Human Prescription Drug

Product NDC51672-1395

Product details

Brand name
Tretinoin
Generic name
Tretinoin
Labeler
Sun Pharmaceutical Industries, Inc.
Dosage form
Cream
Route
Topical
Marketing category
ANDA · ANDA211645
Marketed since
January 22, 2019
Listing expires
December 31, 2026
Pharmacologic class
Retinoid

Active ingredients

Uses, dosage, side effects and warnings for Tretinoin →

Package NDC codes (2)

Package NDCDescriptionSince
51672-1395-01 TUBE in 1 CARTON (51672-1395-0) / 20 g in 1 TUBEJan 22, 2019
51672-1395-91 TUBE in 1 CARTON (51672-1395-9) / 45 g in 1 TUBEJan 22, 2019

Other Tretinoin products