NDC 71335-2898 – Tretinoin

Tretinoin .25 mg/g · Gel · Topical

Human Prescription Drug

Product NDC71335-2898

Product details

Brand name
Tretinoin
Generic name
Tretinoin
Labeler
Bryant Ranch Prepack
Dosage form
Gel
Route
Topical
Marketing category
NDA AUTHORIZED GENERIC · NDA017579
Marketed since
July 12, 2019
Listing expires
December 31, 2026
Pharmacologic class
Retinoid

Active ingredients

Uses, dosage, side effects and warnings for Tretinoin →

Package NDC codes (1)

Package NDCDescriptionSince
71335-2898-11 TUBE in 1 CARTON (71335-2898-1) / 45 g in 1 TUBEOct 21, 2025

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