72493-106 : ZusduriZusduri Kit


NDC: 72493-106
Labeler: Urogen Pharma, Inc
Product Type: Human Prescription Drug
Drug Name:  Zusduri
Dosage Form: Kit
Application #: NDA215793
Rev. Date: 


NDC Package Codes:

  • 72493-106-03: 1 KIT IN 1 CARTON (72493‑106‑03) * 1 POWDER, FOR SOLUTION IN 1 VIAL, SINGLE‑DOSE (72493‑104‑40) * 60 ML IN 1 VIAL, SINGLE‑DOSE (72493‑105‑60)

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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.