# Citalopram

NDC: 70518-4335
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: 20250501

FDA application: ANDA078216

## 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:"70518-4335"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=70518-4335
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=bdc0c228-797a-42dd-8114-aa68c1eb3300