NDC 69911-875 - IDELVION

This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.

Product NDC
69911-875
Package NDCs from labels
69911-875-01
Manufacturer
CSL Behring Lengnau AG | CSL Behring GmbH | CSL Behring LLC
Effective date
2023-06-30
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
IDELVION - CSL Behring Lengnau AG | CSL Behring GmbH | CSL Behring LLCCSL Behring Lengnau AG | CSL Behring GmbH | CSL Behring LLC2023-06-30PLASMA DERIVATIVE

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
69911-875-01IDELVION2.5 mL in 1 VIAL, SINGLE-USEINJECTION, POWDER, LYOPHILIZED,2.5 mL500 [iU] in 2.5mL12

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
69911-875IDELVION (COAGULATION FACTOR IX RECOMBINANT HUMAN) KIT [CSL BEHRING LENGNAU AG]12Unmatched20230706_f74301bf-95e2-44ab-a8b6-98aa07b04683.zip