# Micafungin

NDC: 42023-229
Generic name: Micafungin
Labeler / Manufacturer: Par Health USA, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: New Drug Application (innovator)
Dosage form: INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Routes: INTRAVENOUS
Marketing started: 20210801

FDA application: NDA212156

## Active ingredients

- MICAFUNGIN SODIUM: 10 mg/mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"42023-229"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=42023-229
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=70b3f044-95ca-4503-b669-ed39972592b6
