67457-592 : Arixtra 2.5 mg/.5ml Subcutaneous Injection, Solution


NDC67457-592
Labeler: Mylan Institutional LLC
Product Type: Human Prescription Drug
Drug Name:  Arixtra
Dosage Form: Subcutaneous Injection, Solution
Application #: NDA021345
Rev. Date: 


NDC Package Codes:

  • 67457-592-02: 2 SYRINGE, PLASTIC IN 1 CARTON (67457‑592‑02) > .5 ML IN 1 SYRINGE, PLASTIC (67457‑592‑00)
  • 67457-592-10: 10 SYRINGE, PLASTIC IN 1 CARTON (67457‑592‑10) > .5 ML IN 1 SYRINGE, PLASTIC (67457‑592‑00)

Active Ingredients:

  • Fondaparinux Sodium

Dosage Strength:

  • 2.5 mg/.5mL

Pharmaceutical Classes:

  • Factor Xa Inhibitor [EPC]
  • Factor Xa Inhibitors [MoA]

Related Products:

Based on records with the same trade name.
  • 67457-593 Arixtra 5 mg/.4ml Subcutaneous Injection, Solution by Mylan Institutional LLC
  • 67457-594 Arixtra 7.5 mg/.6ml Subcutaneous Injection, Solution by Mylan Institutional LLC
  • 67457-595 Arixtra 10 mg/.8ml Subcutaneous Injection, Solution by Mylan Institutional LLC
  • 0007-3230 Arixtra 2.5 mg/.5ml Subcutaneous Injection, Solution by Glaxosmithkline LLC
  • 0007-3232 Arixtra 5 mg/.4ml Subcutaneous Injection, Solution by Glaxosmithkline LLC
  • 0007-3234 Arixtra 7.5 mg/.6ml Subcutaneous Injection, Solution by Glaxosmithkline LLC
  • 0007-3236 Arixtra 10 mg/.8ml Subcutaneous Injection, Solution by Glaxosmithkline LLC
  • 54868-5501 Arixtra 7.5 mg/.6ml Subcutaneous Injection, Solution by Physicians Total Care, Inc.

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Note: The RxChat NDC Database uses publicly available data from the FDA and the U.S. National Library of Medicine (NLM); The NLM is not responsible for the data presented and does not endorse or recommend this or any other product. While we make every effort to ensure that the information presented is accurate, you should assume that all results are unvalidated. To report any errors or inconsistencies please contact us.