Home NDC 59137-270 NDC 59137-270 - Ixinity 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 59137-270
Package NDCs from labels 59137-270-01
Manufacturer Medexus Pharma, Inc.
Effective date 2024-04-03
Current FDA listing Not matched in FDA.report NDC product tables DailyMed Labels# Label, Manufacturer, Effective date table Label Manufacturer Effective date Type Ixinity - Medexus Pharma, Inc. Medexus Pharma, Inc. 2024-04-03 HUMAN PRESCRIPTION DRUG LABEL
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 59137-270-01 Ixinity 5 mL in 1 VIAL INJECTION, POWDER, LYOPHILIZED, 5 mL 500 [iU] in 5mL 8
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 59137-270 IXINITY (COAGULATION FACTOR IX (RECOMBINANT)) KIT [MEDEXUS PHARMA, INC.] 8 Unmatched 20240405_26bc221d-c9bc-4aba-92f3-6c21acaaf194.zip