# Escitalopram

NDC: 68788-7461
Generic name: Escitalopram
Labeler / Manufacturer: Preferred Pharmaceuticals, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20120315

FDA application: ANDA078032

## 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:"68788-7461"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=68788-7461
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=3e3a3e36-fb2f-4d9b-bbcf-423bd97c9f88