# Prucalopride

NDC: 0054-0749
Generic name: Prucalopride
Labeler / Manufacturer: Hikma Pharmaceuticals USA Inc
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20250624

FDA application: ANDA217662

## Active ingredients

- PRUCALOPRIDE SUCCINATE: 1 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0054-0749"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0054-0749
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=e1e9e36c-ce5a-4323-9d20-395bb5e80e64