NDC 59651-712 – Tretinoin

Tretinoin .1 mg/g · Gel · Topical

Human Prescription Drug

Product NDC59651-712

Product details

Brand name
Tretinoin
Generic name
Tretinoin
Labeler
Aurobindo Pharma Limited
Dosage form
Gel
Route
Topical
Marketing category
ANDA · ANDA218246
Marketed since
January 13, 2025
Listing expires
December 31, 2026
Pharmacologic class
Retinoid

Active ingredients

Uses, dosage, side effects and warnings for Tretinoin →

Package NDC codes (2)

Package NDCDescriptionSince
59651-712-141 TUBE in 1 CARTON (59651-712-14) / 15 g in 1 TUBEJan 13, 2025
59651-712-461 TUBE in 1 CARTON (59651-712-46) / 45 g in 1 TUBEJan 13, 2025

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