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
- 16714-250_39809802-b48a-ea14-e063-6394a90a1380
- Product NDC
- 16714-250
- Form
- CREAM
- Composition / generic term
- Tretinoin
- Labeler
- NORTHSTAR RX LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20190122
- Source listing expiry
- 20261231
Source-listed ingredients
- TRETINOIN — 1 mg/g
These values do not establish equivalence or a dose recommendation.
Packages
- 1 TUBE in 1 CARTON (16714-250-01) / 20 g in 1 TUBE · 16714-250-01
- 1 TUBE in 1 CARTON (16714-250-02) / 45 g in 1 TUBE · 16714-250-02
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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