United States · FDA National Drug Code directory
Mupirocin
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
- 81033-032_36357344-6528-ef04-e063-6394a90a8fa9
- Product NDC
- 81033-032
- Form
- OINTMENT
- Composition / generic term
- Mupirocin Ointment
- Labeler
- Kesin Pharma Corporation
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20250528
- Source listing expiry
- 20261231
Source-listed ingredients
- MUPIROCIN — 20 mg/g
These values do not establish equivalence or a dose recommendation.
Packages
- 50 TUBE in 1 BOX (81033-032-50) / 1 g in 1 TUBE (81033-032-01) · 81033-032-50
- 100 TUBE in 1 BOX (81033-032-99) / 1 g in 1 TUBE (81033-032-01) · 81033-032-99
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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