# Escitalopram oxalate

NDC: 71610-534
Generic name: escitalopram
Labeler / Manufacturer: Aphena Pharma Solutions - Tennessee, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20121001

FDA application: ANDA078604

## Active ingredients

- ESCITALOPRAM OXALATE: 20 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"71610-534"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=71610-534
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=900b7a2f-23e7-4c78-bd6e-549bbe09883e