# Citalopram

NDC: 42708-019
Generic name: Citalopram Hydrobromide
Labeler / Manufacturer: QPharma, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20041028

FDA application: ANDA077031

## 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:"42708-019"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=42708-019
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=0a967468-3869-4c8c-849f-9fc3a8dcc489