United States · FDA National Drug Code directory
PRUCALOPRIDE
A source-listed medicine record.
Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.
Medicine identity
- Source reference
- 72205-218_89a7fce6-5d3e-4a71-a86c-06d209951c63
- Product NDC
- 72205-218
- Form
- TABLET, FILM COATED
- Composition / generic term
- PRUCALOPRIDE
- Labeler
- Novadoz Pharmaceuticals LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20250624
- Source listing expiry
- 20271231
Source-listed ingredients
- PRUCALOPRIDE SUCCINATE — 1 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 30 TABLET, FILM COATED in 1 BOTTLE (72205-218-30) · 72205-218-30
Source and coverage
Open FDA National Drug Code directory →
Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.
Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.
Browse United States records →