Humalog - 0002-8797-99 - (Insulin lispro)

Alphabetical Index


Drug Information of Humalog

Product NDC: 0002-8797
Proprietary Name: Humalog
Non Proprietary Name: Insulin lispro
Active Ingredient(s): 100    [iU]/mL & nbsp;   Insulin lispro
Administration Route(s): SUBCUTANEOUS
Dosage Form(s): INJECTION, SUSPENSION
Coding System: National Drug Codes(NDC)

Labeler Information of Humalog

Product NDC: 0002-8797
Labeler Name: Eli Lilly and Company
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021017
Marketing Category: NDA
Start Marketing Date: 20080116

Package Information of Humalog

Package NDC: 0002-8797-99
Package Description: 1 SYRINGE in 1 CARTON (0002-8797-99) > 3 mL in 1 SYRINGE

NDC Information of Humalog

NDC Code 0002-8797-99
Proprietary Name Humalog
Package Description 1 SYRINGE in 1 CARTON (0002-8797-99) > 3 mL in 1 SYRINGE
Product NDC 0002-8797
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Insulin lispro
Dosage Form Name INJECTION, SUSPENSION
Route Name 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