Product Details for: Norditropin

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Product Number
Dosage Form
Route of Administration
Strength
Product Presentation
License Type
Proprietary Name
Marketing Status
001
Injection
Subcutaneous
5MG/1.5ML
Multi-Dose Cartridge
351(a)
Norditropin
Disc
002
Injection
Subcutaneous
10MG/1.5ML
Multi-Dose Cartridge
351(a)
Norditropin
Disc
003
Injection
Subcutaneous
15MG/1.5ML
Multi-Dose Cartridge
351(a)
Norditropin
Disc
004
Injection
Subcutaneous
5MG/1.5ML
Autoinjector
351(a)
Norditropin
Disc
005
Injection
Subcutaneous
10MG/1.5ML
Autoinjector
351(a)
Norditropin
Disc
006
Injection
Subcutaneous
15MG/1.5ML
Autoinjector
351(a)
Norditropin
Disc
007
Injection
Subcutaneous
30MG/3ML
Autoinjector
351(a)
Norditropin
Disc
008
Injection
Subcutaneous
5MG/1.5ML
Autoinjector
351(a)
Norditropin
Rx
009
Injection
Subcutaneous
10MG/1.5ML
Autoinjector
351(a)
Norditropin
Rx
010
Injection
Subcutaneous
15MG/1.5ML
Autoinjector
351(a)
Norditropin
Rx
011
Injection
Subcutaneous
30MG/3ML
Autoinjector
351(a)
Norditropin
Rx
Proper Name
somatropin
BLA Number
021148
Applicant
Novo Nordisk Inc.
Original Approval Date
June 20, 2000
Date of First Licensure
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