58394-012 : Xyntha Kit


NDC: 58394-012
Labeler: Wyeth Biopharma Division of Wyeth Pharmaceuticals Inc., a Subsidiary of Pfizer Inc.
Product Type: Plasma Derivative
Drug Name: Xyntha Plasma/Albumin-free
Dosage Form: Kit
Application #: BLA125264
Rev. Date: 


NDC Package Codes:

  • 58394-012-01: 1 KIT IN 1 CARTON (58394‑012‑01) * 4 ML IN 1 SYRINGE (58394‑018‑01) * 1 SWAB IN 1 PACKET * 4 ML IN 1 VIAL, SINGLE‑USE (58394‑112‑01)

Active Ingredients:

  • Antihemophilic Factor (Recombinant
  • Plasma/Albumin-free)

Related Products:

Based on records with the same trade name.
  • 58394-013 Xyntha Kit by Wyeth Biopharma Division of Wyeth Pharmaceuticals Inc., a Subsidiary of Pfizer Inc.
  • 58394-014 Xyntha Kit by Wyeth Biopharma Division of Wyeth Pharmaceuticals Inc., a Subsidiary of Pfizer Inc.
  • 58394-015 Xyntha Kit by Wyeth Biopharma Division of Wyeth Pharmaceuticals Inc., a Subsidiary of Pfizer 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.