# Ethyol

NDC: 83107-030
Generic name: Amifostine
Labeler / Manufacturer: Legacy Pharma USA Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: New Drug Application (innovator)
Dosage form: INJECTION
Routes: INTRAVENOUS
Marketing started: 20260316

FDA application: NDA020221

## Active ingredients

- AMIFOSTINE: 500 mg/10mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"83107-030"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=83107-030
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=a17563f2-d231-4385-bc94-0217be78b89d