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
- 71205-834_a368117c-0e80-4dbc-a0a7-9b88dbfeece3
- Product NDC
- 71205-834
- Form
- CAPSULE, GELATIN COATED
- Composition / generic term
- Lubiprostone
- Labeler
- Proficient Rx LP
- Marketing category
- NDA AUTHORIZED GENERIC
- Marketing start / end (source format)
- 20230101
- Source listing expiry
- 20261231
Source-listed ingredients
- LUBIPROSTONE — 24 ug/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 CAPSULE, GELATIN COATED in 1 BOTTLE (71205-834-00) · 71205-834-00
- 1000 CAPSULE, GELATIN COATED in 1 BOTTLE (71205-834-11) · 71205-834-11
- 30 CAPSULE, GELATIN COATED in 1 BOTTLE (71205-834-30) · 71205-834-30
- 500 CAPSULE, GELATIN COATED in 1 BOTTLE (71205-834-55) · 71205-834-55
- 60 CAPSULE, GELATIN COATED in 1 BOTTLE (71205-834-60) · 71205-834-60
- 240 CAPSULE, GELATIN COATED in 1 BOTTLE (71205-834-64) · 71205-834-64
- 270 CAPSULE, GELATIN COATED in 1 BOTTLE (71205-834-67) · 71205-834-67
- 120 CAPSULE, GELATIN COATED in 1 BOTTLE (71205-834-72) · 71205-834-72
- 180 CAPSULE, GELATIN COATED in 1 BOTTLE (71205-834-78) · 71205-834-78
- 90 CAPSULE, GELATIN COATED in 1 BOTTLE (71205-834-90) · 71205-834-90
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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