12064-010 : Benlysta 400 mg/5ml Intravenous Injection, Powder, Lyophilized, for Solution


NDC: 12064-010
Labeler: Glaxosmithkline Manufacturing Spa
Product Type: Human Prescription Drug
Drug Name:  Benlysta
Dosage Form: Intravenous Injection, Powder, Lyophilized, for Solution
Application #: BLA125370
Rev. Date: 


NDC Package Codes:

  • 12064-010-00: 1 VIAL IN 1 CARTON (12064‑010‑00) > 5 ML IN 1 VIAL

Active Ingredients:

  • Belimumab

Dosage Strength:

  • 400 mg/5mL

Pharmaceutical Classes:

  • Decreased B Lymphocyte Activation [PE]
  • B Lymphocyte Stimulator-specific Inhibitor [EPC]
  • B Lymphocyte Stimulator-directed Antibody Interactions [MoA]

Related Products:

Based on records with the same trade name.
  • 12064-009 Benlysta 120 mg/1.5ml Intravenous Injection, Powder, Lyophilized, for Solution by Glaxosmithkline Manufacturing Spa
  • 49401-088 Benlysta 200 mg/ml Subcutaneous Solution by Human Genome Sciences, Inc.
  • 49401-101 Benlysta 120 mg/1.5ml Intravenous Injection, Powder, Lyophilized, for Solution by Human Genome Sciences, Inc.
  • 49401-102 Benlysta 400 mg/5ml Intravenous Injection, Powder, Lyophilized, for Solution by Human Genome Sciences, Inc.

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Related Discussions:

Migraines associated to Benlysta use?
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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.