United States · FDA National Drug Code directory
Prucalopride succinate
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
- 70069-821_7b3acc62-d656-47b8-91d2-5b30cd699fbd
- Product NDC
- 70069-821
- Form
- TABLET
- Composition / generic term
- Prucalopride succinate
- Labeler
- Somerset Therapeutics, LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20250624
- Source listing expiry
- 20261231
Source-listed ingredients
- PRUCALOPRIDE SUCCINATE — 1 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 1 BOTTLE in 1 BOTTLE (70069-821-01) / 30 TABLET in 1 BOTTLE · 70069-821-01
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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