# Escitalopram Oral Solution

NDC: 68999-729
Generic name: Escitalopram Oral
Labeler / Manufacturer: Chartwell Governmental & Specialty RX, LLC.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: SOLUTION
Routes: ORAL
Marketing started: 20230612

FDA application: ANDA090477

## 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:"68999-729"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=68999-729
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=45ed4d16-6358-40a1-9352-319e58f55e5d