United States · FDA National Drug Code directory

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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
51672-5263_4cd6638c-db25-e28b-e063-6294a90a4a9a
Product NDC
51672-5263
Form
OINTMENT
Composition / generic term
Desoximetasone
Labeler
Sun Pharmaceutical Industries, Inc.
Marketing category
NDA
Marketing start / end (source format)
19850117
Source listing expiry
20271231

Source-listed ingredients

  • DESOXIMETASONE — .5 mg/g

These values do not establish equivalence or a dose recommendation.

Packages

  • 1 TUBE in 1 CARTON (51672-5263-1) / 15 g in 1 TUBE · 51672-5263-1
  • 1 TUBE in 1 CARTON (51672-5263-2) / 30 g in 1 TUBE · 51672-5263-2
  • 10 TUBE in 1 CARTON (51672-5263-5) / 5 g in 1 TUBE · 51672-5263-5
  • 1 TUBE in 1 CARTON (51672-5263-7) / 100 g in 1 TUBE · 51672-5263-7

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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