# Citalopram

NDC: 70518-2553
Generic name: citalopram
Labeler / Manufacturer: REMEDYREPACK INC.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20200122

FDA application: ANDA077042

## Active ingredients

- CITALOPRAM HYDROBROMIDE: 10 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"70518-2553"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=70518-2553
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=f79f878e-99fb-4757-8abb-931af1fa9e2b