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
- 68682-515_c4ef7e4d-9c2e-4022-b7ab-b55962c1a58a
- Product NDC
- 68682-515
- Form
- GEL
- Composition / generic term
- Tretinoin
- Labeler
- Oceanside Pharmaceuticals
- Marketing category
- NDA AUTHORIZED GENERIC
- Marketing start / end (source format)
- 20231201
- Source listing expiry
- 20271231
Source-listed ingredients
- TRETINOIN — .8 mg/g
These values do not establish equivalence or a dose recommendation.
Packages
- 1 BOTTLE, PUMP in 1 CARTON (68682-515-95) / 50 g in 1 BOTTLE, PUMP · 68682-515-95
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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