# escitalopram

NDC: 33342-053
Generic name: escitalopram
Labeler / Manufacturer: Macleods Pharmaceuticals Limited
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: SOLUTION
Routes: ORAL
Marketing started: 20160331

FDA application: ANDA202754

## Active ingredients

- ESCITALOPRAM OXALATE: 5 mg/5mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"33342-053"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=33342-053
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=4d5c3142-b850-49b9-9f5c-81fe15ea7bfb