On this page

Nuwiq

Antihemophilic Factor (Recombinant)

351(a) Standalone BLA

Overview

Source: Purple Book
Proprietary name
Nuwiq
Proper name
Antihemophilic Factor (Recombinant)
Licence type
351(a)
BLA number
125555
Applicant
Octapharma Pharmazeutika Produktionsges.m.b.H.
Center
CBER
Presentations
8
First licensure
—

Presentations

Source: Purple Book
Every strength and presentation recorded in the Purple Book for this product.
Strength Dosage form Route Presentation Status Licensed
1000IU For Injection Intravenous Vial Rx September 4, 2015
1500IU For Injection Intravenous Single-Dose Vial Rx December 7, 2021
2000IU For Injection Intravenous Single-Dose Vial Rx September 4, 2015
2500IU For Injection Intravenous Single-Dose Vial Rx July 7, 2017
250IU For Injection Intravenous Single-Dose Vial Rx September 4, 2015
3000IU For Injection Intravenous Single-Dose Vial Rx July 7, 2017
4000IU For Injection Intravenous Single-Dose Vial Rx July 7, 2017
500IU For Injection Intravenous Vial Rx September 4, 2015

Sources for this page

Purple Book FDA Licence type, presentations, reference product, exclusivity