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
- 70166-355_313090ef-ad58-1103-e063-6394a90a7d75
- Product NDC
- 70166-355
- Form
- OINTMENT
- Composition / generic term
- Mupirocin
- Labeler
- Lohxa
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20180526
- Source listing expiry
- 20261231
Source-listed ingredients
- MUPIROCIN — 20 mg/g
These values do not establish equivalence or a dose recommendation.
Packages
- 100 TUBE in 1 CARTON (70166-355-10) / 1 g in 1 TUBE · 70166-355-10
- 50 TUBE in 1 CARTON (70166-355-50) / 1 g in 1 TUBE · 70166-355-50
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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