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
- 0781-8159_0145490a-4ba4-4b33-8602-4a6e9ca52ff2
- Product NDC
- 0781-8159
- Form
- TABLET, FILM COATED
- Composition / generic term
- PRUCALOPRIDE
- Labeler
- Sandoz Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20250613
- Source listing expiry
- 20261231
Source-listed ingredients
- PRUCALOPRIDE SUCCINATE — 2 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 30 TABLET, FILM COATED in 1 BOTTLE (0781-8159-31) · 0781-8159-31
Source and coverage
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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.
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