# CITALOPRAM

NDC: 42806-021
Generic name: citalopram
Labeler / Manufacturer: Epic Pharma, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20110520

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:"42806-021"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=42806-021
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=08b6d5da-5919-4760-9e16-3b478a14d6d7