# Imiquimod

NDC: 68462-536
Generic name: Imiquimod
Labeler / Manufacturer: Glenmark Pharmaceuticals Inc., USA
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CREAM
Routes: TOPICAL
Marketing started: 20120306

FDA application: ANDA201994

## Active ingredients

- IMIQUIMOD: 50 mg/g

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"68462-536"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=68462-536
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=663e39a9-a29e-473f-89ec-4c7c6bc27b8a