United States · FDA National Drug Code directory

Fondaparinux Sodium

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
67457-582_9448af58-144f-4611-a462-e8cb12cc7362
Product NDC
67457-582
Form
INJECTION, SOLUTION
Composition / generic term
fondaparinux sodium
Labeler
Mylan Institutional LLC
Marketing category
NDA AUTHORIZED GENERIC
Marketing start / end (source format)
20150105
Source listing expiry
20271231

Source-listed ingredients

  • FONDAPARINUX SODIUM — 2.5 mg/.5mL

These values do not establish equivalence or a dose recommendation.

Packages

  • 10 SYRINGE, GLASS in 1 CARTON (67457-582-10) / .5 mL in 1 SYRINGE, GLASS (67457-582-00) · 67457-582-10

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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Fondaparinux Sodium — United States | Molindra Medicines