# CITALOPRAM HYDROBROMIDE

NDC: 76282-208
Generic name: CITALOPRAM
Labeler / Manufacturer: Exelan Pharmaceuticals Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20121001

FDA application: ANDA077534

## Active ingredients

- CITALOPRAM HYDROBROMIDE: 40 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"76282-208"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=76282-208
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=a8e8fde2-8392-4d5b-902b-e2b9dd55a02d