# Citalopram

NDC: 68999-540
Generic name: Citalopram
Labeler / Manufacturer: Chartwell Governmental & Specialty RX, LLC.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: SOLUTION
Routes: ORAL
Marketing started: 20060614

FDA application: ANDA077629

## Active ingredients

- CITALOPRAM HYDROBROMIDE: 10 mg/5mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"68999-540"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=68999-540
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=3114274f-d81f-4b1f-8f17-35db9eee2ffe