# Escitalopram

NDC: 0615-8477
Generic name: Escitalopram Oxalate
Labeler / Manufacturer: NCS HealthCare of KY, LLC dba Vangard Labs
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20120911

FDA application: ANDA090432

## Active ingredients

- ESCITALOPRAM OXALATE: 20 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0615-8477"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0615-8477
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=ac9ede0c-7912-4e7d-83b3-964feee61215