# escitalopram

NDC: 13668-137
Generic name: escitalopram
Labeler / Manufacturer: Torrent Pharmaceuticals Limited
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20120911

FDA application: ANDA090939

## 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:"13668-137"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=13668-137
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=068bb338-23f3-4278-958b-c34b40456024