Product Details for: Omvoh

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Product Number
Dosage Form
Route of Administration
Strength
Product Presentation
License Type
Proprietary Name
Marketing Status
001
Injection
Intravenous
300MG/15ML (20MG/ML)
Single-Dose Vial
351(a)
Omvoh
Rx
002
Injection
Subcutaneous
100MG/ML
Pre-Filled Syringe
351(a)
Omvoh
Rx
003
Injection
Subcutaneous
100MG/ML
Autoinjector
351(a)
Omvoh
Rx
004
Injection
Subcutaneous
200MG/2ML (100MG/ML)
Autoinjector
351(a)
Omvoh
Rx
005
Injection
Subcutaneous
200MG/2ML (100MG/ML)
Pre-Filled Syringe
351(a)
Omvoh
Rx
Proper Name
mirikizumab-mrkz
BLA Number
761279
Applicant
Eli Lilly and Company
Original Approval Date
October 26, 2023
Date of First Licensure
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