# Escitalopram Oxalate

NDC: 31722-569
Generic name: Escitalopram Oxalate
Labeler / Manufacturer: Camber Pharmaceuticals, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: SOLUTION
Routes: ORAL
Marketing started: 20120612

FDA application: ANDA202221

## 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:"31722-569"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=31722-569
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=82d793ee-4039-45fc-ac83-4bd5235f00aa