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
- 43598-168_8f55941d-f7c6-4a16-ae76-c2cd1ab7d607
- Product NDC
- 43598-168
- Form
- CAPSULE, GELATIN COATED
- Composition / generic term
- Lubiprostone
- Labeler
- Dr. Reddy's Laboratories Inc.
- Marketing category
- NDA AUTHORIZED GENERIC
- Marketing start / end (source format)
- 20230101
- Source listing expiry
- 20271231
Source-listed ingredients
- LUBIPROSTONE — 24 ug/1
These values do not establish equivalence or a dose recommendation.
Packages
- 60 CAPSULE, GELATIN COATED in 1 BOTTLE (43598-168-60) · 43598-168-60
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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