Lexapro - 54868-4775-0 - (escitalopram oxalate)

Alphabetical Index


Drug Information of Lexapro

Product NDC: 54868-4775
Proprietary Name: Lexapro
Non Proprietary Name: escitalopram oxalate
Active Ingredient(s): 20    mg/1 & nbsp;   escitalopram oxalate
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Lexapro

Product NDC: 54868-4775
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021323
Marketing Category: NDA
Start Marketing Date: 20090415

Package Information of Lexapro

Package NDC: 54868-4775-0
Package Description: 10 TABLET in 1 BOTTLE, PLASTIC (54868-4775-0)

NDC Information of Lexapro

NDC Code 54868-4775-0
Proprietary Name Lexapro
Package Description 10 TABLET in 1 BOTTLE, PLASTIC (54868-4775-0)
Product NDC 54868-4775
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name escitalopram oxalate
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20090415
Marketing Category Name NDA
Labeler Name Physicians Total Care, Inc.
Substance Name ESCITALOPRAM OXALATE
Strength Number 20
Strength Unit mg/1
Pharmaceutical Classes Serotonin Reuptake Inhibitor [EPC],Serotonin Uptake Inhibitors [MoA]

Complete Information of Lexapro


General Information