# Escitalopram Oxalate

NDC: 33342-037
Generic name: Escitalopram Oxalate
Labeler / Manufacturer: Macleods Pharmaceuticals Limited
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20120911

FDA application: ANDA202210

## Active ingredients

- ESCITALOPRAM OXALATE: 10 mg/21

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"33342-037"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=33342-037
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=24b43cb4-1a26-44a2-b1d8-a40239eb5c7c