United States · FDA National Drug Code directory

Tretinoin

A source-listed medicine record.

Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.

Medicine identity

Source reference: 71335-2898_ca82745d-d880-4b6a-af76-97b8ce1519ab
Product NDC: 71335-2898
Form: GEL
Composition / generic term: Tretinoin
Labeler: Bryant Ranch Prepack
Marketing category: NDA AUTHORIZED GENERIC
Marketing start / end (source format): 20190712
Source listing expiry: 20261231

Source-listed ingredients

TRETINOIN — .25 mg/g

These values do not establish equivalence or a dose recommendation.

Packages

1 TUBE in 1 CARTON (71335-2898-1) / 45 g in 1 TUBE · 71335-2898-1

Source and coverage

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Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.

Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.

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