NDC 0944-3942

Hemofil M 500 [iU] per 10 mL kit

On the label: Takeda Pharmaceuticals America, Inc..

United States: 2

Where it's made

FactoryWhereRoleLast FDA inspection
Baxalta Us Inc.Thousand Oaks, CA, United StatesMakes it Not inspected on record
Baxalta Us Inc.Los Angeles, CA, United StatesMakes it Not inspected on record

Product details

Generic drug
Antihemophilic Factor Human: every company that makes it
Form
kit
Strength
500 [iU] per 10 mL
Approval
BLA BLA101448
On the market since
Feb 23, 1988
Package NDCs
0944-3942-02 0944-3943-01 64764-516-10
Official label
DailyMed (National Library of Medicine), updated Mar 6, 2025

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