# MOTEGRITY

NDC: 54092-547
Generic name: PRUCALOPRIDE
Labeler / Manufacturer: Takeda Pharmaceuticals America, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: New Drug Application (innovator)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20181214

FDA application: NDA210166

## 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:"54092-547"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=54092-547
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=bca1e4c6-4b2b-4876-8ab3-654629c4ff1b
