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
- 68462-299_098145f1-cb92-4222-8069-72fbf92fce9f
- Product NDC
- 68462-299
- Form
- OINTMENT
- Composition / generic term
- Alclometasone Dipropionate
- Labeler
- Glenmark Pharmaceuticals Inc., USA
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20090730
- Source listing expiry
- 20261231
Source-listed ingredients
- ALCLOMETASONE DIPROPIONATE — .5 mg/g
These values do not establish equivalence or a dose recommendation.
Packages
- 15 g in 1 TUBE (68462-299-17) · 68462-299-17
- 45 g in 1 TUBE (68462-299-47) · 68462-299-47
- 60 g in 1 TUBE (68462-299-65) · 68462-299-65
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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