# CITALOPRAM HYDROBROMIDE

NDC: 43353-112
Generic name: CITALOPRAM
Labeler / Manufacturer: Aphena Pharma Solutions - Tennessee, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20121001

FDA application: ANDA077534

## 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:"43353-112"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=43353-112
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=7307df53-d570-4e26-971d-e97522ccce7f