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
68788-4069_d6819051-4748-479e-8b53-c298edcbd410
Product NDC
68788-4069
Form
CREAM
Composition / generic term
tretinoin
Labeler
Preferred Pharmaceuticals Inc.
Marketing category
ANDA
Marketing start / end (source format)
20260128
Source listing expiry
20271231

Source-listed ingredients

  • TRETINOIN — .25 mg/g

These values do not establish equivalence or a dose recommendation.

Packages

  • 1 TUBE in 1 CARTON (68788-4069-2) / 20 g in 1 TUBE · 68788-4069-2

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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