0173-0821 : Arzerra 20 mg/ml Intravenous Injection, Solution


NDC0173-0821
Labeler: Glaxosmithkline LLC
Product Type: Human Prescription Drug
Drug Name:  Arzerra
Dosage Form: Intravenous Injection, Solution
Application #: BLA125326
Rev. Date: 


NDC Package Codes:

  • 0173-0821-01: 1 VIAL IN 1 CARTON (0173‑0821‑01) > 50 ML IN 1 VIAL
  • 0173-0821-33: 3 VIAL IN 1 CARTON (0173‑0821‑33) > 5 ML IN 1 VIAL (0173‑0821‑02)

Active Ingredients:

  • Ofatumumab

Dosage Strength:

  • 20 mg/mL

Pharmaceutical Classes:

  • CD20-directed Cytolytic Antibody [EPC]

Related Products:

Based on records with the same trade name.
  • 0078-0669 Arzerra 20 mg/ml Intravenous Injection, Solution by Novartis Pharmaceuticals Corporation
  • 0078-0690 Arzerra 20 mg/ml Intravenous Injection, Solution by Novartis Pharmaceuticals Corporation
  • 63379-023 Arzerra 20 mg/ml Intravenous Injection, Solution by Glaxo Operations Uk Ltd

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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.