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
- 63187-151_a22d9ce1-ccc1-4955-939c-b74e110cffa5
- Product NDC
- 63187-151
- Form
- OINTMENT
- Composition / generic term
- Mupirocin
- Labeler
- Proficient Rx LP
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20050923
- Source listing expiry
- 20261231
Source-listed ingredients
- MUPIROCIN — 20 mg/g
These values do not establish equivalence or a dose recommendation.
Packages
- 1 TUBE in 1 CARTON (63187-151-22) / 22 g in 1 TUBE · 63187-151-22
Source and coverage
Open FDA National Drug Code directory →
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.
Browse United States records →