Humalog - 0002-7510-01 - (Insulin lispro)

Alphabetical Index


Drug Information of Humalog

Product NDC: 0002-7510
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: 0002-7510
Labeler Name: Eli Lilly and Company
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020563
Marketing Category: NDA
Start Marketing Date: 19960724

Package Information of Humalog

Package NDC: 0002-7510-01
Package Description: 1 VIAL in 1 CARTON (0002-7510-01) > 10 mL in 1 VIAL

NDC Information of Humalog

NDC Code 0002-7510-01
Proprietary Name Humalog
Package Description 1 VIAL in 1 CARTON (0002-7510-01) > 10 mL in 1 VIAL
Product NDC 0002-7510
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Insulin lispro
Dosage Form Name INJECTION, SOLUTION
Route Name INTRAVENOUS; SUBCUTANEOUS
Start Marketing Date 19960724
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