Product Details for: Humatrope

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Product Number
Dosage Form
Route of Administration
Strength
Product Presentation
License Type
Proprietary Name
Marketing Status
001
For Injection
Subcutaneous
2MG
Single-Dose Vial
351(a)
Humatrope
Disc
004
For Injection
Subcutaneous
5MG
Single-Dose Vial
351(a)
Humatrope
Disc
005
For Injection
Subcutaneous
6MG
Multi-Dose Cartridge
351(a)
Humatrope
Rx
006
For Injection
Subcutaneous
12MG
Multi-Dose Cartridge
351(a)
Humatrope
Rx
007
For Injection
Subcutaneous
24MG
Multi-Dose Cartridge
351(a)
Humatrope
Rx
Proper Name
somatropin
BLA Number
019640
Applicant
Eli Lilly and Company
Original Approval Date
June 23, 1987
Date of First Licensure
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