# Citalopram

NDC: 70518-4114
Generic name: Citalopram Hydrobromide
Labeler / Manufacturer: REMEDYREPACK INC.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20240626

FDA application: ANDA077031

## Active ingredients

- CITALOPRAM HYDROBROMIDE: 20 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"70518-4114"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=70518-4114
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=625a78b2-4751-4ca5-91b6-7c85fd9f8c2e