FDA.reportPublic FDA data

NDC 70504-0276 - 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
70504-0276
Package NDCs from labels
70504-0276-1
Manufacturer
Aptevo BioTherapeutics LLC
Effective date
2021-02-23
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Ixinity - Aptevo BioTherapeutics LLCAptevo BioTherapeutics LLC2021-02-23HUMAN PRESCRIPTION DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
70504-0276-1Ixinity5 mL in 1 VIALINJECTION, POWDER, LYOPHILIZED,5 mL2000 [iU] in 5mL10

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
70504-0276IXINITY (COAGULATION FACTOR IX (RECOMBINANT)) KIT [APTEVO BIOTHERAPEUTICS LLC]10Unmatched20210305_9521898c-61aa-44ab-8ab8-84274ca19943.zip