Product Details for: Opdualag
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Product Number
Dosage Form
Route of Administration
Strength
Product Presentation
License Type
Proprietary Name
Marketing Status
001
Injection
Intravenous
240MG, 80MG/20ML (12MG, 4MG/ML)
Single-Dose Vial
351(a)
Opdualag
Rx
Proper Name
nivolumab and relatlimab-rmbw
nivolumab and relatlimab-rmbw
BLA Number
761234
761234
Applicant
Bristol-Myers Squibb Company
Bristol-Myers Squibb Company
Original Approval Date
March 18, 2022
March 18, 2022
Date of First Licensure