# Micafungin

NDC: 71288-028
Generic name: Micafungin sodium
Labeler / Manufacturer: Meitheal Pharmaceuticals Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Routes: INTRAVENOUS
Marketing started: 20220928

FDA application: ANDA215381

## Active ingredients

- MICAFUNGIN SODIUM: 50 mg/5mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"71288-028"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=71288-028
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=579ff093-0359-4e0e-a6ea-2b6adac80bf0