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
- 16714-270_3629fc6a-a4f9-926e-e063-6294a90affdb
- Product NDC
- 16714-270
- Form
- CREAM
- Composition / generic term
- tretinoin
- Labeler
- NORTHSTAR RX LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20230105
- 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 (16714-270-01) / 20 g in 1 TUBE · 16714-270-01
- 1 TUBE in 1 CARTON (16714-270-02) / 45 g in 1 TUBE · 16714-270-02
Source and coverage
Open FDA National Drug Code directory →
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.
Browse United States records →