NDC 62032-413 – Tretinoin

Tretinoin .05 g/100g · Gel · Topical

Human Prescription Drug

Product NDC62032-413

Product details

Brand name
Tretinoin
Generic name
Tretinoin
Labeler
Obagi Cosmeceuticals LLC
Dosage form
Gel
Route
Topical
Marketing category
NDA AUTHORIZED GENERIC · NDA022070
Marketed since
June 19, 2014
Listing expires
December 31, 2026
Pharmacologic class
Retinoid

Active ingredients

Uses, dosage, side effects and warnings for Tretinoin →

Package NDC codes (1)

Package NDCDescriptionSince
62032-413-2020 g in 1 TUBE (62032-413-20)Jun 19, 2014

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