Home NDC 49591-300 NDC 49591-300 - WinRho SDF 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 49591-300
Package NDCs from labels 49591-300-13, 49591-300-51
Manufacturer Kamada Ltd.
Effective date 2026-04-16
Current FDA listing Not matched in FDA.report NDC product tables DailyMed Labels# Label, Manufacturer, Effective date table Label Manufacturer Effective date Type WinRho SDF - Kamada Ltd. Kamada Ltd. 2026-04-16 PLASMA DERIVATIVE
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 49591-300-13 WinRho SDF 13 mL in 1 VIAL, GLASS INJECTION, SOLUTION 13 6 49591-300-51 WinRho SDF 1 in 1 CARTON INJECTION, SOLUTION 1 6
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 49591-300 WINRHO SDF (HUMAN RHO(D) IMMUNE GLOBULIN) INJECTION, SOLUTION [KAMADA LTD.] 3 2 package rows 20240529_fdb8ec91-f3ec-40c5-9337-23cc5bcc4c6e.zip