Lantus - 54868-6231-0 - (insulin glargine)

Alphabetical Index


Drug Information of Lantus

Product NDC: 54868-6231
Proprietary Name: Lantus
Non Proprietary Name: insulin glargine
Active Ingredient(s): 100    [iU]/mL & nbsp;   insulin glargine
Administration Route(s): SUBCUTANEOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Lantus

Product NDC: 54868-6231
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021081
Marketing Category: NDA
Start Marketing Date: 20110207

Package Information of Lantus

Package NDC: 54868-6231-0
Package Description: 5 CARTRIDGE in 1 CARTON (54868-6231-0) > 3 mL in 1 CARTRIDGE

NDC Information of Lantus

NDC Code 54868-6231-0
Proprietary Name Lantus
Package Description 5 CARTRIDGE in 1 CARTON (54868-6231-0) > 3 mL in 1 CARTRIDGE
Product NDC 54868-6231
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name insulin glargine
Dosage Form Name INJECTION, SOLUTION
Route Name SUBCUTANEOUS
Start Marketing Date 20110207
Marketing Category Name NDA
Labeler Name Physicians Total Care, Inc.
Substance Name INSULIN GLARGINE
Strength Number 100
Strength Unit [iU]/mL
Pharmaceutical Classes Insulin [Chemical/Ingredient],Insulin Analog [EPC]

Complete Information of Lantus


General Information