# Citalopram Hydrobromide

NDC: 55700-787
Generic name: Citalopram Hydrobromide
Labeler / Manufacturer: Quality Care Products, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20190830
Marketing ended: 20270930
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:"55700-787"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=55700-787
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=e22fe468-5d9e-4ec7-a69b-4988e0b8acbd