Product Details for: Raptiva

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Product Number
Dosage Form
Route of Administration
Strength
Product Presentation
License Type
Proprietary Name
Marketing Status
001
Injection
Subcutaneous
125MG
Single-Dose Vial
351(a)
Raptiva
Disc
Proper Name
efalizumab
BLA Number
125075
Applicant
Genentech, Inc.
Original Approval Date
October 27, 2003
Date of First Licensure
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