United States · FDA National Drug Code directory
Mometasone Furoate
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
- 71205-413_c08fcb0d-7fff-4d90-aeb8-e912b930bf3d
- Product NDC
- 71205-413
- Form
- OINTMENT
- Composition / generic term
- Mometasone Furoate
- Labeler
- Proficient Rx LP
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20080718
- Source listing expiry
- 20261231
Source-listed ingredients
- MOMETASONE FUROATE — 1 mg/g
These values do not establish equivalence or a dose recommendation.
Packages
- 1 TUBE in 1 CARTON (71205-413-15) / 15 g in 1 TUBE · 71205-413-15
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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