United States · FDA National Drug Code directory
Alclometasone Dipropionate
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
- 51672-1316_3c44a51b-8abe-ceae-e063-6294a90a482c
- Product NDC
- 51672-1316
- Form
- OINTMENT
- Composition / generic term
- Alclometasone dipropionate
- Labeler
- Sun Pharmaceutical Industries, Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20040729
- Source listing expiry
- 20261231
Source-listed ingredients
- ALCLOMETASONE DIPROPIONATE — .5 mg/g
These values do not establish equivalence or a dose recommendation.
Packages
- 1 TUBE in 1 CARTON (51672-1316-1) / 15 g in 1 TUBE · 51672-1316-1
- 1 TUBE in 1 CARTON (51672-1316-3) / 60 g in 1 TUBE · 51672-1316-3
- 5 g in 1 TUBE (51672-1316-5) · 51672-1316-5
- 1 TUBE in 1 CARTON (51672-1316-6) / 45 g in 1 TUBE · 51672-1316-6
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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