NDC 21922-042 – Tretinoin

Tretinoin .6 mg/g · Gel · Topical

Human Prescription Drug

Product NDC21922-042

Product details

Brand name
Tretinoin
Generic name
Tretinoin
Labeler
Encube Ethicals, Inc.
Dosage form
Gel
Route
Topical
Marketing category
ANDA · ANDA215609
Marketed since
April 16, 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
21922-042-401 BOTTLE, PUMP in 1 CARTON (21922-042-40) / 50 g in 1 BOTTLE, PUMPApr 16, 2026

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