50242-159 : Lunsumio 1 mg/ml Intravenous Concentrate


NDC: 50242-159
Labeler: Genentech, Inc.
Product Type: Human Prescription Drug
Drug Name:  Lunsumio
Dosage Form: Intravenous Concentrate
Application #: BLA761263
Rev. Date: 


NDC Package Codes:

  • 50242-159-01: 1 VIAL IN 1 CARTON (50242‑159‑01) / 1 ML IN 1 VIAL

Active Ingredients:

  • Mosunetuzumab

Dosage Strength:

  • 1 mg/mL

Related Products:

Based on records with the same trade name.
  • 50242-142 Lunsumio 30 mg/30ml Intravenous Concentrate by Genentech, 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.