# Ivermectin

NDC: 24338-119
Generic name: Ivermectin
Labeler / Manufacturer: Azurity Pharmaceuticals, Inc.
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: LOTION
Routes: TOPICAL
Marketing started: 20260811

FDA application: ANDA210720

## Active ingredients

- IVERMECTIN: 5 mg/g

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"24338-119"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=24338-119
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=58c9cc4d-b1f3-1b6f-e063-6294a90ab597