# Escitalopram Oxalate

NDC: 68645-520
Generic name: Escitalopram
Labeler / Manufacturer: Legacy Pharmaceutical Packaging, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20160616
Marketing ended: 20270831
FDA application: ANDA078604

## Active ingredients

- ESCITALOPRAM OXALATE: 20 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"68645-520"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=68645-520
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=9c68f89b-1d34-4735-9631-817f012935d7