# Citalopram

NDC: 43063-481
Generic name: Citalopram
Labeler / Manufacturer: PD-Rx Pharmaceuticals, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20071018

FDA application: ANDA078216

## 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:"43063-481"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=43063-481
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=df929b3f-0cda-4a75-96d3-22e6b0edbbc9