NDC 51672-1407 – Tretinoin

Tretinoin .25 mg/g · Cream · Topical

Human Prescription Drug

Product NDC51672-1407

Product details

Brand name
Tretinoin
Generic name
Tretinoin
Labeler
Sun Pharmaceutical Industries, Inc.
Dosage form
Cream
Route
Topical
Marketing category
ANDA · ANDA215713
Marketed since
January 5, 2023
Listing expires
December 31, 2026
Pharmacologic class
Retinoid

Active ingredients

Uses, dosage, side effects and warnings for Tretinoin →

Package NDC codes (2)

Package NDCDescriptionSince
51672-1407-01 TUBE in 1 CARTON (51672-1407-0) / 20 g in 1 TUBEJan 5, 2023
51672-1407-91 TUBE in 1 CARTON (51672-1407-9) / 45 g in 1 TUBEJan 5, 2023

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