NDC 69238-2323 – Tretinoin

Tretinoin .8 mg/g · Gel · Topical

Human Prescription Drug

Product NDC69238-2323

Product details

Brand name
Tretinoin
Generic name
Tretinoin
Labeler
Amneal Pharmaceuticals NY LLC
Dosage form
Gel
Route
Topical
Marketing category
ANDA · ANDA217497
Marketed since
May 15, 2026
Listing expires
December 31, 2027
Pharmacologic class
Retinoid

Active ingredients

Uses, dosage, side effects and warnings for Tretinoin →

Package NDC codes (1)

Package NDCDescriptionSince
69238-2323-11 BOTTLE, PUMP in 1 CARTON (69238-2323-1) / 50 g in 1 BOTTLE, PUMPMay 15, 2026

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