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
0781-3454_3d5a4b69-462b-7e51-e063-6294a90a0721
Product NDC
0781-3454
Form
INJECTION
Composition / generic term
Fondaparinux Sodium
Labeler
Sandoz Inc.
Marketing category
ANDA
Marketing start / end (source format)
20190618
Source listing expiry
20261231

Source-listed ingredients

  • FONDAPARINUX SODIUM — 5 mg/.4mL

These values do not establish equivalence or a dose recommendation.

Packages

  • 2 SYRINGE in 1 CARTON (0781-3454-12) / .4 mL in 1 SYRINGE (0781-3454-94) · 0781-3454-12
  • 10 SYRINGE in 1 CARTON (0781-3454-95) / .4 mL in 1 SYRINGE (0781-3454-94) · 0781-3454-95

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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