Lubiprostone

NDC 51407-745 · Golden State Medical Supply, Inc.

Generic namelubiprostone

Dosage formCAPSULE, GELATIN COATED

RouteORAL

Active ingredient(s)LUBIPROSTONE

Strength24 ug/1

Pharmacologic classChloride Channel Activator [EPC], Chloride Channel Activators [MoA]

Marketing categoryNDA AUTHORIZED GENERIC

Packages

51407-745-60 — 60 CAPSULE, GELATIN COATED in 1 BOTTLE (51407-745-60)

FDA lists these products with the same active ingredient.

0406-6424 — Lubiprostone, 0480-3479 — Lubiprostone, 0480-4138 — Lubiprostone, 23635-508 — lubiprostone, 23635-524 — lubiprostone, 31722-403 — lubiprostone, 31722-404 — lubiprostone, 43598-163 — Lubiprostone, 43598-168 — Lubiprostone, 51407-744 — lubiprostone, 60687-816 — Lubiprostone, 60687-827 — Lubiprostone, 63304-351 — lubiprostone, 63304-352 — lubiprostone, 64764-080 — lubiprostone, 64764-240 — lubiprostone, 69339-162 — LUBIPROSTONE, 69339-163 — LUBIPROSTONE, 70710-1641 — Lubiprostone, 70710-1642 — Lubiprostone, +21 more

From the FDA National Drug Code Directory, retrieved August 24, 2026. Product listings are submitted by labelers; FDA does not verify them.