72579-121 : Tevimbra 10 mg/ml Intravenous Injection, Solution, Concentrate


NDC: 72579-121
Labeler: Beigene USA, Inc.
Product Type: Human Prescription Drug
Drug Name:  Tevimbra
Dosage Form: Intravenous Injection, Solution, Concentrate
Application #: BLA761232
Rev. Date: 


NDC Package Codes:

  • 72579-121-01: 1 VIAL, GLASS IN 1 CARTON (72579‑121‑01) / 10 ML IN 1 VIAL, GLASS

Active Ingredients:

  • Tislelizumab

Dosage Strength:

  • 10 mg/mL

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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.