Product Details for: Lartruvo

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Product Number
Dosage Form
Route of Administration
Strength
Product Presentation
License Type
Proprietary Name
Marketing Status
001
Injection
Intravenous
500MG/50ML (10MG/ML)
Single-Dose Vial
351(a)
Lartruvo
Disc
002
Injection
Intravenous
190MG/19ML (10MG/ML)
Single-Dose Vial
351(a)
Lartruvo
Disc
Proper Name
olaratumab
BLA Number
761038
Applicant
Eli Lilly and Company
Original Approval Date
October 19, 2016
Date of First Licensure
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