United States · FDA National Drug Code directory
Fluocinonide
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
- 51672-1264_46a43966-e83f-a3cc-e063-6394a90af22d
- Product NDC
- 51672-1264
- Form
- OINTMENT
- Composition / generic term
- Fluocinonide
- Labeler
- Sun Pharmaceutical Industries, Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 19990630
- Source listing expiry
- 20261231
Source-listed ingredients
- FLUOCINONIDE — .5 mg/g
These values do not establish equivalence or a dose recommendation.
Packages
- 1 TUBE in 1 CARTON (51672-1264-1) / 15 g in 1 TUBE · 51672-1264-1
- 1 TUBE in 1 CARTON (51672-1264-2) / 30 g in 1 TUBE · 51672-1264-2
- 1 TUBE in 1 CARTON (51672-1264-3) / 60 g in 1 TUBE · 51672-1264-3
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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