# PRUCALOPRIDE

NDC: 0781-8159
Generic name: PRUCALOPRIDE
Labeler / Manufacturer: Sandoz Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20250613

FDA application: ANDA218963

## Active ingredients

- PRUCALOPRIDE SUCCINATE: 2 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0781-8159"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0781-8159
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=6325308c-4b0f-4926-bb85-b63db614533d