Product Details for: Degevma

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Product Number
Dosage Form
Route of Administration
Strength
Product Presentation
License Type
Proprietary Name
Marketing Status
001
Injection
Subcutaneous
120MG/1.7ML (70MG/ML)
Single-Dose Vial
351(k) Interchangeable
Degevma
Rx
Proper Name
denosumab-adet
Reference Product Proper Name
denosumab
Reference Product Properietary Name
Xgeva
BLA Number
761481
Applicant
Teva Pharmaceuticals, Inc.
Original Approval Date
September 25, 2026
Date of First Licensure
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