Home NDC 0026-4950 NDC 0026-4950 - Jivi 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 0026-4950
Package NDCs from labels 0026-4950-01, 0026-4950-99
Manufacturer Bayer HealthCare LLC
Effective date 2026-03-02
Current FDA listing Not matched in FDA.report NDC product tables DailyMed Labels# Label, Manufacturer, Effective date table Label Manufacturer Effective date Type Jivi - Bayer HealthCare LLC Bayer HealthCare LLC 2026-03-02 PLASMA DERIVATIVE
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 0026-4950-01 Jivi 5 mL in 1 VIAL, SINGLE-USE INJECTION, POWDER, LYOPHILIZED, 5 mL 4000 [iU] in 5mL 13 0026-4950-99 Jivi 5 mL in 1 VIAL INJECTION, POWDER, LYOPHILIZED, 5 mL 4000 [iU] in 5mL 13
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 0026-4950 JIVI (ANTIHEMOPHILIC FACTOR (RECOMBINANT) PEGYLATED-AUCL) KIT [BAYER HEALTHCARE LLC] 11 Unmatched 20250529_f04e5bd5-d7e2-453b-a407-2616d81a695d.zip