# Prucalopride

NDC: 0406-6301
Generic name: Prucalopride
Labeler / Manufacturer: SpecGx LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20250624

FDA application: ANDA219193

## Active ingredients

- PRUCALOPRIDE: 1 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0406-6301"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0406-6301
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=70fced73-c25b-46cb-ad30-19328e6130c3