NDC 0944-3945 - HEMOFIL M

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
0944-3945
Package NDCs from labels
0944-3945-01
Manufacturer
Takeda Pharmaceuticals America, Inc. | BAXALTA US Inc.
Effective date
2025-03-06
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
HEMOFIL M - Takeda Pharmaceuticals America, Inc. | BAXALTA US Inc.Takeda Pharmaceuticals America, Inc. | BAXALTA US Inc.2025-03-06PLASMA DERIVATIVE

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
0944-3945-01HEMOFIL M10 mL in 1 BOTTLEPOWDER, FOR SOLUTION10 mL1000 [iU] in 10mL15

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
0944-3945HEMOFIL M (ANTIHEMOPHILIC FACTOR HUMAN) KIT [TAKEDA PHARMACEUTICALS AMERICA, INC.]15Unmatched20250309_b8953ff7-3bba-4a0b-a486-f26fb81f05d9.zip

DailyMed Socrata Ingredients#