# Escitalopram Oxalate

NDC: 33342-036
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: 5 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"33342-036"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=33342-036
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=24b43cb4-1a26-44a2-b1d8-a40239eb5c7c