Drugplain

RECOMBINATE

antihemophilic factor recombinant · KIT · Takeda Pharmaceuticals America, Inc.

1 Recall on Record
Plain English

RECOMBINATE is a kit containing antihemophilic factor recombinant. Manufactured by Takeda Pharmaceuticals America, Inc..

Key Facts

Brand Name
RECOMBINATE
Generic Name
antihemophilic factor recombinant
NDC Code (Product)
0944-2845
Manufacturer
Takeda Pharmaceuticals America, Inc.
Dosage Form
KIT
Marketing Status
Application #
BLA103375
Marketing Start
03/15/2010

Recall History

1 Recall on Record
Class II07/30/2025

Cardinal Health Inc.

CGMP Deviations - Product was exposed to temperatures outside the product's labeled storage requirements.

OngoingVoluntary: Firm initiated

Frequently Asked Questions

What is RECOMBINATE used for?

RECOMBINATE contains antihemophilic factor recombinant. It is a kit taken as directed. Consult your doctor for specific uses.

Is RECOMBINATE a controlled substance?

RECOMBINATE is not classified as a controlled substance by the DEA.

What is the generic name for RECOMBINATE?

The generic name for RECOMBINATE is antihemophilic factor recombinant. There are 6 other brand versions of antihemophilic factor recombinant.

What is the NDC code for RECOMBINATE ?

The NDC (National Drug Code) for RECOMBINATE is 0944-2845, listed by Takeda Pharmaceuticals America, Inc..

Product NDC

0944-2845

Package NDC

0944-2845-10

Not medical advice. Always consult your doctor or pharmacist before making any medication decisions.

Data from openFDA · Public domain (CC0 1.0)