Lantus - 54868-4626-0 - (insulin glargin)

Alphabetical Index


Drug Information of Lantus

Product NDC: 54868-4626
Proprietary Name: Lantus
Non Proprietary Name: insulin glargin
Active Ingredient(s): 100    [iU]/mL & nbsp;   insulin glargin
Administration Route(s): SUBCUTANEOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Lantus

Product NDC: 54868-4626
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021081
Marketing Category: NDA
Start Marketing Date: 20020604

Package Information of Lantus

Package NDC: 54868-4626-0
Package Description: 1 VIAL, GLASS in 1 CARTON (54868-4626-0) > 10 mL in 1 VIAL, GLASS

NDC Information of Lantus

NDC Code 54868-4626-0
Proprietary Name Lantus
Package Description 1 VIAL, GLASS in 1 CARTON (54868-4626-0) > 10 mL in 1 VIAL, GLASS
Product NDC 54868-4626
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name insulin glargin
Dosage Form Name INJECTION, SOLUTION
Route Name SUBCUTANEOUS
Start Marketing Date 20020604
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