# Citalopram Hydrobromide

NDC: 17856-0564
Generic name: Citalopram Hydrobromide
Labeler / Manufacturer: ATLANTIC BIOLOGICALS CORP.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: SOLUTION
Routes: ORAL
Marketing started: 20190531

FDA application: ANDA201450

## Active ingredients

- CITALOPRAM HYDROBROMIDE: 10 mg/5mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"17856-0564"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=17856-0564
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=2640311d-8b88-4513-9c80-a08390b8142a