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
85534-0038_5792ff59-c571-3f87-e063-6394a90a5995
Product NDC
85534-0038
Form
OINTMENT
Composition / generic term
Mupirocin
Labeler
HAWAII REPACK, INC.
Marketing category
ANDA
Marketing start / end (source format)
20091030
Source listing expiry
20271231

Source-listed ingredients

  • MUPIROCIN — 20 mg/g

These values do not establish equivalence or a dose recommendation.

Packages

  • 1 TUBE in 1 CARTON (85534-0038-0) / 22 g in 1 TUBE · 85534-0038-0

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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