United States · FDA National Drug Code directory
Imiquimod
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
- 51672-4174_48e9d045-e9a2-8452-e063-6294a90af1e9
- Product NDC
- 51672-4174
- Form
- CREAM
- Composition / generic term
- Imiquimod
- Labeler
- Sun Pharmaceutical Industries, Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20210126
- Source listing expiry
- 20271231
Source-listed ingredients
- IMIQUIMOD — 37.5 mg/g
These values do not establish equivalence or a dose recommendation.
Packages
- 28 PACKET in 1 CARTON (51672-4174-6) / .25 g in 1 PACKET (51672-4174-8) · 51672-4174-6
- 1 BOTTLE, PUMP in 1 CARTON (51672-4174-9) / 7.5 g in 1 BOTTLE, PUMP · 51672-4174-9
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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