# CITALOPRAM

NDC: 60429-175
Generic name: citalopram
Labeler / Manufacturer: Golden State Medical Supply, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20050429

FDA application: ANDA077045

## Active ingredients

- CITALOPRAM HYDROBROMIDE: 40 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"60429-175"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=60429-175
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=f3a26d92-b662-4896-82eb-261948042408