# Micafungin

NDC: 70710-1725
Generic name: Micafungin
Labeler / Manufacturer: Zydus Pharmaceuticals USA Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Routes: INTRAVENOUS
Marketing started: 20230410

FDA application: ANDA215241

## Active ingredients

- MICAFUNGIN SODIUM: 20 mg/mL

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"70710-1725"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=70710-1725
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=29f17423-5787-47d0-a83b-bbdc0198fbfa