United States · FDA National Drug Code directory

Lubiprostone

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
51407-744_57b2423d-ecf1-abe5-e063-6394a90ad2a6
Product NDC
51407-744
Form
CAPSULE, GELATIN COATED
Composition / generic term
lubiprostone
Labeler
Golden State Medical Supply, Inc.
Marketing category
NDA AUTHORIZED GENERIC
Marketing start / end (source format)
20080429
Source listing expiry
20271231

Source-listed ingredients

  • LUBIPROSTONE — 8 ug/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 60 CAPSULE, GELATIN COATED in 1 BOTTLE (51407-744-60) · 51407-744-60

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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