# Miconazole Nitrate

NDC: 51672-2035
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: 19970113

FDA application: ANDA074444

## Active ingredients

- MICONAZOLE NITRATE: 20 mg/g

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"51672-2035"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=51672-2035
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=6b34d0be-4bcd-4dff-b732-7fbd46765019