# Citalopram Hydrobromide

NDC: 55700-851
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: 20200320
Marketing ended: 20261031
FDA application: ANDA078216

## Active ingredients

- CITALOPRAM HYDROBROMIDE: 20 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"55700-851"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=55700-851
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=6fc110ba-87e7-404e-9e00-b680f354c7b0