# Citalopram Hydrobromide

NDC: 80425-0309
Generic name: Citalopram Hydrobromide
Labeler / Manufacturer: Advanced Rx Pharmacy of Tennessee, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20230406

FDA application: ANDA077031

## Active ingredients

- CITALOPRAM HYDROBROMIDE: 10 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"80425-0309"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=80425-0309
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=f8b06b55-f6a2-2438-e053-6394a90a530a