# Citalopram

NDC: 0054-0062
Generic name: Citalopram
Labeler / Manufacturer: Hikma Pharmaceuticals USA Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: SOLUTION
Routes: ORAL
Marketing started: 20040525

FDA application: ANDA077043

## 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:"0054-0062"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0054-0062
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=29408d84-7b00-4cee-969c-8095f8083ff5