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Nuwiq
Antihemophilic Factor (Recombinant)
351(a) Standalone BLA
Overview
Source: Purple BookProprietary 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| 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 |