Omnitrope - 0781-3004-26 - (Somatropin)

Alphabetical Index


Drug Information of Omnitrope

Product NDC: 0781-3004
Proprietary Name: Omnitrope
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 Omnitrope

Product NDC: 0781-3004
Labeler Name: Sandoz Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021426
Marketing Category: NDA
Start Marketing Date: 20060530

Package Information of Omnitrope

Package NDC: 0781-3004-26
Package Description: 5 CARTRIDGE in 1 CARTON (0781-3004-26) > 1.5 mL in 1 CARTRIDGE

NDC Information of Omnitrope

NDC Code 0781-3004-26
Proprietary Name Omnitrope
Package Description 5 CARTRIDGE in 1 CARTON (0781-3004-26) > 1.5 mL in 1 CARTRIDGE
Product NDC 0781-3004
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Somatropin
Dosage Form Name INJECTION, SOLUTION
Route Name SUBCUTANEOUS
Start Marketing Date 20060530
Marketing Category Name NDA
Labeler Name Sandoz Inc
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 Omnitrope


General Information