HUMATROPE - 0002-8147-01 - (Somatropin)

Alphabetical Index


Drug Information of HUMATROPE

Product NDC: 0002-8147
Proprietary Name: HUMATROPE
Non Proprietary Name: Somatropin
Active Ingredient(s):    & nbsp;   Somatropin
Administration Route(s): INTRAMUSCULAR; SUBCUTANEOUS
Dosage Form(s): KIT
Coding System: National Drug Codes(NDC)

Labeler Information of HUMATROPE

Product NDC: 0002-8147
Labeler Name: Eli Lilly and Company
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA019640
Marketing Category: NDA
Start Marketing Date: 20060127

Package Information of HUMATROPE

Package NDC: 0002-8147-01
Package Description: 1 TRAY in 1 CARTON (0002-8147-01) > 1 KIT in 1 TRAY * 2.88 mL in 1 CARTRIDGE (0002-7554-01) * 2.88 mL in 1 SYRINGE (0002-7618-01)

NDC Information of HUMATROPE

NDC Code 0002-8147-01
Proprietary Name HUMATROPE
Package Description 1 TRAY in 1 CARTON (0002-8147-01) > 1 KIT in 1 TRAY * 2.88 mL in 1 CARTRIDGE (0002-7554-01) * 2.88 mL in 1 SYRINGE (0002-7618-01)
Product NDC 0002-8147
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Somatropin
Dosage Form Name KIT
Route Name INTRAMUSCULAR; SUBCUTANEOUS
Start Marketing Date 20060127
Marketing Category Name NDA
Labeler Name Eli Lilly and Company
Substance Name
Strength Number
Strength Unit
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Complete Information of HUMATROPE


General Information