# Escitalopram

NDC: 59746-280
Generic name: Escitalopram Oxalate
Labeler / Manufacturer: Jubilant Cadista Pharmacuticals Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20231201

FDA application: ANDA202280

## Active ingredients

- ESCITALOPRAM OXALATE: 10 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"59746-280"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=59746-280
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=2db02476-325f-ee47-a7e5-b5aed56c364c