Product Details for: Lumoxiti

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Product Number
Dosage Form
Route of Administration
Strength
Product Presentation
License Type
Proprietary Name
Marketing Status
001
For Injection
Intravenous
1MG
Single-Dose Vial
351(a)
Lumoxiti
Disc
Proper Name
moxetumomab pasudotox-tdfk
BLA Number
761104
Applicant
AstraZeneca AB
Original Approval Date
September 13, 2018
Date of First Licensure
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