Product Details for: Kedbumin

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Product Number
Dosage Form
Route of Administration
Strength
Product Presentation
License Type
Proprietary Name
Marketing Status
001
Injection
Intravenous
12.5G/50ML
Single-Dose Vial
351(a)
Kedbumin
Rx
002
Injection
Intravenous
25G/100ML
Single-Dose Vial
351(a)
Kedbumin
Rx
Proper Name
Albumin (Human)
BLA Number
125384
Applicant
Kedrion Biopharma Inc.
Original Approval Date
June 3, 2011
Date of First Licensure
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