United States · FDA National Drug Code directory

Ethyol

A source-listed medicine record.

Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.

Medicine identity

Source reference
83107-030_4c20479c-d75a-a0c7-e063-6394a90a9e59
Product NDC
83107-030
Form
INJECTION
Composition / generic term
Amifostine
Labeler
Legacy Pharma USA Inc.
Marketing category
NDA
Marketing start / end (source format)
20260316
Source listing expiry
20271231

Source-listed ingredients

  • AMIFOSTINE — 500 mg/10mL

These values do not establish equivalence or a dose recommendation.

Packages

  • 3 VIAL, SINGLE-DOSE in 1 CARTON (83107-030-02) / 10 mL in 1 VIAL, SINGLE-DOSE (83107-030-01) · 83107-030-02

Source and coverage

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Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.

Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.

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