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
- 68682-272_36b25854-8ed2-8f45-e063-6294a90a8b46
- Product NDC
- 68682-272
- Form
- CREAM
- Composition / generic term
- imiquimod
- Labeler
- Oceanside Pharmacueticals
- Marketing category
- NDA
- Marketing start / end (source format)
- 20180627
- Source listing expiry
- 20261231
Source-listed ingredients
- IMIQUIMOD — 37.5 mg/g
These values do not establish equivalence or a dose recommendation.
Packages
- 1 BOTTLE, PUMP in 1 CARTON (68682-272-75) / 7.5 g in 1 BOTTLE, PUMP · 68682-272-75
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 →