escitalopram
escitalopram is listed in the FDA National Drug Code directory with 39 NDC codes, marketed under brand names including escitalopram, ESCITALOPRAM OXALATE, Escitalopram oxalate. Available dosage forms: tablet, film coated, tablet, capsule, solution.
Drug Details
- Generic Name
- escitalopram
- Brand Names
- escitalopram, ESCITALOPRAM OXALATE, Escitalopram oxalate
- Application Number
- ANDA090939
- Sponsor
- Major Pharmaceuticals
- NDC Codes
- 39
- Dosage Forms
- TABLET, FILM COATED, TABLET, CAPSULE, SOLUTION
- 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) in adults. 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 tablets are a selective serotonin reuptake inhibitor (SSRI) indicated for: • treatment of major depressive disorder (MDD) in adults and pediatric patients 12 years of age and older () • treatment of generalized anxiety disorder (GAD) in adults ()