25682-028 : Ultomiris 1100 mg/11ml Intravenous Solution, Concentrate


NDC: 25682-028
Labeler: Alexion Pharmaceuticals Inc.
Product Type: Human Prescription Drug
Drug Name:  Ultomiris
Dosage Form: Intravenous Solution, Concentrate
Application #: BLA761108
Rev. Date: 


NDC Package Codes:

  • 25682-028-01: 1 VIAL, GLASS IN 1 CARTON (25682‑028‑01) > 11 ML IN 1 VIAL, GLASS

Active Ingredients:

  • Ravulizumab

Dosage Strength:

  • 1100 mg/11mL

Pharmaceutical Classes:

  • Complement Inhibitor [EPC]
  • Complement Inhibitors [MoA]

Related Products:

Based on records with the same trade name.
  • 25682-022 Ultomiris 300 mg/30ml Intravenous Solution, Concentrate by Alexion Pharmaceuticals Inc.
  • 25682-025 Ultomiris 300 mg/3ml Intravenous Solution, Concentrate by Alexion Pharmaceuticals Inc.
  • 25682-031 UltomirisUltomiris Kit by Alexion Pharmaceuticals 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.