# Miconazole Nitrate

NDC: 51672-2070
Generic name: Miconazole Nitrate
Labeler / Manufacturer: Sun Pharmaceutical Industries, Inc.
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CREAM
Routes: VAGINAL
Marketing started: 20050302

FDA application: ANDA076773

## Active ingredients

- MICONAZOLE NITRATE: 40 mg/g

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"51672-2070"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=51672-2070
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=eaca3e39-6ea0-4d7e-803c-db22024ad9f9