United States · FDA National Drug Code directory

Calcitrene

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
51672-5278_5698b4f1-b04f-1b1f-e063-6394a90ae022
Product NDC
51672-5278
Form
OINTMENT
Composition / generic term
Calcipotriene
Labeler
Sun Pharmaceutical Industries, Inc.
Marketing category
ANDA
Marketing start / end (source format)
20100324
Source listing expiry
20271231

Source-listed ingredients

  • CALCIPOTRIENE — .05 mg/g

These values do not establish equivalence or a dose recommendation.

Packages

  • 1 TUBE in 1 CARTON (51672-5278-3) / 60 g in 1 TUBE · 51672-5278-3
  • 1 TUBE in 1 CARTON (51672-5278-4) / 120 g in 1 TUBE · 51672-5278-4
  • 10 TUBE in 1 CARTON (51672-5278-5) / 5 g in 1 TUBE · 51672-5278-5

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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