United States · FDA National Drug Code directory

GRAFAPEX

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
59137-365_2d06b03c-17aa-0492-e063-6294a90abd8f
Product NDC
59137-365
Form
INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Composition / generic term
treosulfan
Labeler
Medexus Pharma, Inc.
Marketing category
NDA
Marketing start / end (source format)
20250128
Source listing expiry
20261231

Source-listed ingredients

  • TREOSULFAN — 5000 mg/5g

These values do not establish equivalence or a dose recommendation.

Packages

  • 1 VIAL in 1 CARTON (59137-365-01) / 5 g in 1 VIAL · 59137-365-01

Source and coverage

Open FDA National Drug Code directory

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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