escitalopram oxalate

FDA Drug Profile — escitalopram oxalate

escitalopram oxalate is listed in the FDA National Drug Code directory with 11 NDC codes, marketed under brand name including escitalopram oxalate. Available dosage forms: tablet, tablet, film coated, powder.

Drug Details

Generic Name
escitalopram oxalate
Brand Names
escitalopram oxalate
Application Number
ANDA090939
Sponsor
Pharmasource Meds, LLC
NDC Codes
11
Dosage Forms
TABLET, TABLET, FILM COATED, POWDER
Routes
ORAL
Active Ingredients
ESCITALOPRAM OXALATE

Indications and Usage

1 INDICATIONS AND USAGE Escitalopram tablets are indicated for the treatment of: major depressive disorder (MDD) in adults and pediatric patients 12 years of age and older. generalized anxiety disorder (GAD) inadults. Additional pediatric use information is approved for AbbVie Inc.’s LEXAPRO (escitalopram) tablets. However, due to AbbVie Inc.’s marketing exclusivity rights, this drug product is not labeled with that information. Escitalopram oxalate is a selective serotonin reuptake inhibitor (SSRI) indicated for the: treatment of major depressive disorder (MDD) in adults and pediatric patients 12 years of age and older ( 1 ) treatment of generalized anxiety disorder (GAD) in adults ( 1 )