# Prucalopride

NDC: 70954-596
Generic name: Prucalopride
Labeler / Manufacturer: ANI Pharmaceuticals, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20241226

FDA application: ANDA218492

## 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:"70954-596"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=70954-596
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=6d82dfbd-f171-4045-9f7a-268e189a658a