Lexapro - 63629-2981-1 - (ESCITALOPRAM OXALATE)

Alphabetical Index


Drug Information of Lexapro

Product NDC: 63629-2981
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, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Lexapro

Product NDC: 63629-2981
Labeler Name: Bryant Ranch Prepack
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021323
Marketing Category: NDA
Start Marketing Date: 20020814

Package Information of Lexapro

Package NDC: 63629-2981-1
Package Description: 30 TABLET, FILM COATED in 1 BOTTLE (63629-2981-1)

NDC Information of Lexapro

NDC Code 63629-2981-1
Proprietary Name Lexapro
Package Description 30 TABLET, FILM COATED in 1 BOTTLE (63629-2981-1)
Product NDC 63629-2981
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name ESCITALOPRAM OXALATE
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20020814
Marketing Category Name NDA
Labeler Name Bryant Ranch Prepack
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