# Citalopram Hydrobromide

NDC: 65862-074
Generic name: Citalopram Hydrobromide
Labeler / Manufacturer: Aurobindo Pharma Limited
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: SOLUTION
Routes: ORAL
Marketing started: 20060828

FDA application: ANDA077812

## 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:"65862-074"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=65862-074
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=e7a2cbdd-1bdb-4e59-a3dd-298a189753ae