Drugplain

ALTUVIIIO

Antihemophilic Factor (Recombinant), Fc-VWF-XTEN Fusion Protein-ehtl · KIT · Bioverativ Therapeutics Inc.

No Recall History
Plain English

ALTUVIIIO is a kit containing antihemophilic factor (recombinant), fc-vwf-xten fusion protein-ehtl. Manufactured by Bioverativ Therapeutics Inc..

Key Facts

Brand Name
ALTUVIIIO
Generic Name
Antihemophilic Factor (Recombinant), Fc-VWF-XTEN Fusion Protein-ehtl
NDC Code (Product)
71104-979
Manufacturer
Bioverativ Therapeutics Inc.
Dosage Form
KIT
Marketing Status
Application #
BLA125771
Marketing Start
02/22/2023

Recall History

No Recall History

Frequently Asked Questions

What is ALTUVIIIO used for?

ALTUVIIIO contains Antihemophilic Factor (Recombinant), Fc-VWF-XTEN Fusion Protein-ehtl. It is a kit taken as directed. Consult your doctor for specific uses.

Is ALTUVIIIO a controlled substance?

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

What is the generic name for ALTUVIIIO?

The generic name for ALTUVIIIO is Antihemophilic Factor (Recombinant), Fc-VWF-XTEN Fusion Protein-ehtl. There are no other listed brand versions of Antihemophilic Factor (Recombinant), Fc-VWF-XTEN Fusion Protein-ehtl.

What is the NDC code for ALTUVIIIO ?

The NDC (National Drug Code) for ALTUVIIIO is 71104-979, listed by Bioverativ Therapeutics Inc..

Product NDC

71104-979

Package NDC

71104-979-01

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

Data from openFDA · Public domain (CC0 1.0)