Humalog - 0002-8799-99 - (Insulin lispro)

Alphabetical Index


Drug Information of Humalog

Product NDC: 0002-8799
Proprietary Name: Humalog
Non Proprietary Name: Insulin lispro
Active Ingredient(s): 100    [iU]/mL & nbsp;   Insulin lispro
Administration Route(s): INTRAVENOUS; SUBCUTANEOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Humalog

Product NDC: 0002-8799
Labeler Name: Eli Lilly and Company
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020563
Marketing Category: NDA
Start Marketing Date: 20080116

Package Information of Humalog

Package NDC: 0002-8799-99
Package Description: 1 SYRINGE in 1 CARTON (0002-8799-99) > 3 mL in 1 SYRINGE

NDC Information of Humalog

NDC Code 0002-8799-99
Proprietary Name Humalog
Package Description 1 SYRINGE in 1 CARTON (0002-8799-99) > 3 mL in 1 SYRINGE
Product NDC 0002-8799
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Insulin lispro
Dosage Form Name INJECTION, SOLUTION
Route Name INTRAVENOUS; SUBCUTANEOUS
Start Marketing Date 20080116
Marketing Category Name NDA
Labeler Name Eli Lilly and Company
Substance Name INSULIN LISPRO
Strength Number 100
Strength Unit [iU]/mL
Pharmaceutical Classes Insulin [Chemical/Ingredient],Insulin Analog [EPC]

Complete Information of Humalog


General Information