United States · FDA National Drug Code directory

Amitiza

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
64764-080_c2ca8178-4da1-42d1-a8b9-ff66dca82649
Product NDC
64764-080
Form
CAPSULE, GELATIN COATED
Composition / generic term
lubiprostone
Labeler
Takeda Pharmaceuticals America, Inc.
Marketing category
NDA
Marketing start / end (source format)
20060131 / 20270331

Source-listed ingredients

  • LUBIPROSTONE — 8 ug/1

These values do not establish equivalence or a dose recommendation.

Packages

Package details are not available in this snapshot.

Source and coverage

Open FDA National Drug Code directory

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.

Browse United States records →