# Citalopram Hydrobromide

NDC: 51655-043
Generic name: Citalopram Hydrobromide
Labeler / Manufacturer: Northwind Health Company, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20210324

FDA application: ANDA078216

## Active ingredients

- CITALOPRAM HYDROBROMIDE: 10 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"51655-043"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=51655-043
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=c133fc77-6c8a-d2b1-e053-2995a90ab5f7