Humalog - 0002-7511-99 - (Insulin lispro)

Alphabetical Index


Drug Information of Humalog

Product NDC: 0002-7511
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: 0002-7511
Labeler Name: Eli Lilly and Company
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021017
Marketing Category: NDA
Start Marketing Date: 19991222

Package Information of Humalog

Package NDC: 0002-7511-99
Package Description: 1 VIAL in 1 CARTON (0002-7511-99) > 10 mL in 1 VIAL

NDC Information of Humalog

NDC Code 0002-7511-99
Proprietary Name Humalog
Package Description 1 VIAL in 1 CARTON (0002-7511-99) > 10 mL in 1 VIAL
Product NDC 0002-7511
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Insulin lispro
Dosage Form Name INJECTION, SUSPENSION
Route Name SUBCUTANEOUS
Start Marketing Date 19991222
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