49401-088 : Benlysta 200 mg/ml Subcutaneous Solution


NDC: 49401-088
Labeler: Human Genome Sciences, Inc.
Product Type: Human Prescription Drug
Drug Name:  Benlysta
Dosage Form: Subcutaneous Solution
Application #: BLA761043
Rev. Date: 


NDC Package Codes:

  • 49401-088-02: 1 SYRINGE IN 1 CARTON (49401‑088‑02) > 1 ML IN 1 SYRINGE (49401‑088‑01)
  • 49401-088-35: 4 SYRINGE IN 1 CARTON (49401‑088‑35) > 1 ML IN 1 SYRINGE (49401‑088‑01)
  • 49401-088-47: 4 SYRINGE IN 1 CARTON (49401‑088‑47) > 1 ML IN 1 SYRINGE (49401‑088‑42)
  • 49401-088-50: 1 SYRINGE IN 1 CARTON (49401‑088‑50) > 1 ML IN 1 SYRINGE (49401‑088‑42)
  • 49401-088-61: 1 SYRINGE IN 1 CARTON (49401‑088‑61) > 1 ML IN 1 SYRINGE

Active Ingredients:

  • Belimumab

Dosage Strength:

  • 200 mg/mL

Pharmaceutical Classes:

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

Related Products:

Based on records with the same trade name.
  • 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.
  • 12064-009 Benlysta 120 mg/1.5ml Intravenous Injection, Powder, Lyophilized, for Solution by Glaxosmithkline Manufacturing Spa
  • 12064-010 Benlysta 400 mg/5ml Intravenous Injection, Powder, Lyophilized, for Solution by Glaxosmithkline Manufacturing Spa

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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.