# Ivermectin

NDC: 51672-4230
Generic name: Ivermectin
Labeler / Manufacturer: Sun Pharmaceutical Industries, Inc.
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: LOTION
Routes: TOPICAL
Marketing started: 20200506

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:"51672-4230"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=51672-4230
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=dd2c66e6-bd50-46df-a335-26215d02d13b