Product Details for: Neumega

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Product Number
Dosage Form
Route of Administration
Strength
Product Presentation
License Type
Proprietary Name
Marketing Status
001
For Injection
Subcutaneous
5MG
Single-Dose Vial
351(a)
Neumega
Disc
Proper Name
oprelvekin
BLA Number
103694
Applicant
Wyeth Pharmaceuticals Inc.
Original Approval Date
November 25, 1997
Date of First Licensure
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