Product Details for: Adbry
RETURN TO SEARCH RESULTS
PRODUCT LABEL
Grayed out Product Label links indicate that there is no product label available for the product.
Product Number
Dosage Form
Route of Administration
Strength
Product Presentation
License Type
Proprietary Name
Marketing Status
001
Injection
Subcutaneous
150MG/ML
Pre-Filled Syringe
351(a)
Adbry
Rx
002
Injection
Subcutaneous
300MG/2ML
Autoinjector
351(a)
Adbry
Rx
Proper Name
tralokinumab-ldrm
tralokinumab-ldrm
BLA Number
761180
761180
Applicant
LEO Pharma A/S
LEO Pharma A/S
Original Approval Date
December 27, 2021
December 27, 2021
Date of First Licensure