# Escitalopram Oxalate

NDC: 69097-847
Generic name: Escitalopram
Labeler / Manufacturer: Cipla USA Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20160616

FDA application: ANDA078604

## Active ingredients

- ESCITALOPRAM OXALATE: 5 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"69097-847"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=69097-847
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=31ce0b82-58fe-44f3-8887-c55d8df1b773