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Norditropin - 0169-7705-92 - (somatropin)

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Drug Information of Norditropin

Product NDC: 0169-7705
Proprietary Name: Norditropin
Non Proprietary Name: somatropin
Active Ingredient(s): 10    mg/1.5mL & nbsp;   somatropin
Administration Route(s): SUBCUTANEOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Norditropin

Product NDC: 0169-7705
Labeler Name: Novo Nordisk
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021148
Marketing Category: NDA
Start Marketing Date: 20060102

Package Information of Norditropin

Package NDC: 0169-7705-92
Package Description: 1 SYRINGE, PLASTIC in 1 CARTON (0169-7705-92) > 1.5 mL in 1 SYRINGE, PLASTIC

NDC Information of Norditropin

NDC Code 0169-7705-92
Proprietary Name Norditropin
Package Description 1 SYRINGE, PLASTIC in 1 CARTON (0169-7705-92) > 1.5 mL in 1 SYRINGE, PLASTIC
Product NDC 0169-7705
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name somatropin
Dosage Form Name INJECTION, SOLUTION
Route Name SUBCUTANEOUS
Start Marketing Date 20060102
Marketing Category Name NDA
Labeler Name Novo Nordisk
Substance Name SOMATROPIN
Strength Number 10
Strength Unit mg/1.5mL
Pharmaceutical Classes Recombinant Human Growth Hormone [EPC],Recombinant Human Growth Hormones [Chemical/Ingredient]

Complete Information of Norditropin


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