NDC 65219-562 - IDACIO

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
65219-562
Package NDCs from labels
65219-562-01
Manufacturer
Fresenius Kabi USA, LLC | Merck Serono S.A.
Effective date
2024-10-15
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
IDACIO - Fresenius Kabi USA, LLC | Merck Serono S.A.Fresenius Kabi USA, LLC | Merck Serono S.A.2024-10-15HUMAN PRESCRIPTION DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
65219-562-01IDACIO0.8 mL in 1 VIAL, GLASSINJECTION0.8 mL40 mg in 0.8mL1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
65219-562IDACIO (ADALIMUMAB-AACF) KIT [FRESENIUS KABI USA, LLC]1Unmatched20241209_08dbaffe-9d05-43cf-b24b-b44ade8685fc.zip