# Citalopram

NDC: 72162-2517
Generic name: Citalopram Hydrobromide
Labeler / Manufacturer: Bryant Ranch Prepack
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:"72162-2517"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=72162-2517
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=0bc0e09e-0f1d-4d52-b8fe-3ef8a2e5ea52