# Citalopram Hydrobromide

NDC: 68071-1830
Generic name: Citalopram Hydrobromide
Labeler / Manufacturer: NuCare Pharmaceuticals,Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20071018

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:"68071-1830"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=68071-1830
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=c584909b-e7b2-7108-e053-2995a90a2f54