# Imiquimod

NDC: 68682-272
Generic name: imiquimod
Labeler / Manufacturer: Oceanside Pharmacueticals
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: New Drug Application (innovator)
Dosage form: CREAM
Routes: TOPICAL
Marketing started: 20180627

FDA application: NDA022483

## Active ingredients

- IMIQUIMOD: 37.5 mg/g

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"68682-272"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=68682-272
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=d86eeb0e-70e0-4c72-aaa3-37daa1d8611e