NDC 68516-4610 - Alphanate

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
68516-4610
Package NDCs from labels
68516-4610-2
Manufacturer
GRIFOLS USA, LLC | Grifols Biologicals LLC | LABORATORIOS GRIFOLS SA
Effective date
2025-05-22
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Alphanate - GRIFOLS USA, LLC | Grifols Biologicals LLC | LABORATORIOS GRIFOLS SAGRIFOLS USA, LLC | Grifols Biologicals LLC | LABORATORIOS GRIFOLS SA2025-05-22PLASMA DERIVATIVE

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
68516-4610-2Alphanate10 mL in 1 VIALINJECTION, POWDER, LYOPHILIZED,10 mL2000 [iU] in 10mL26
68516-4610-2Alphanate10 mL in 1 VIALINJECTION, POWDER, LYOPHILIZED,10 mL2000 [iU] in 10mL26

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
68516-4610ALPHANATE (ANTIHEMOPHILIC FACTOR/VON WILLEBRAND FACTOR COMPLEX (HUMAN)) KIT [GRIFOLS USA, LLC]25Unmatched20231009_5a7aea94-654c-4113-9014-c3137de0a931.zip

DailyMed Socrata Ingredients#