Product Details for: Opdivo Qvantig
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Product Number
Dosage Form
Route of Administration
Strength
Product Presentation
License Type
Proprietary Name
Marketing Status
001
Injection
Subcutaneous
600MG/5ML;10,000UNITS/5ML (120MG/2,000UNITS/ML)
Single-Dose Vial
351(a)
Opdivo Qvantig
Rx
002
Injection
Subcutaneous
300MG/2.5ML;5,000UNITS/2.5ML (120MG/2,000UNITS/ML)
Single-Dose Vial
351(a)
Opdivo Qvantig
Rx
Proper Name
nivolumab and hyaluronidase-nvhy
nivolumab and hyaluronidase-nvhy
BLA Number
761381
761381
Applicant
Bristol-Myers Squibb Company
Bristol-Myers Squibb Company
Original Approval Date
December 27, 2024
December 27, 2024
Date of First Licensure