Lubiprostone

NDC 82804-304 · Proficient Rx LP

Generic nameLubiprostone

Dosage formCAPSULE, GELATIN COATED

RouteORAL

Active ingredient(s)LUBIPROSTONE

Strength24 ug/1

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

Marketing categoryANDA

Packages

82804-304-60 — 60 CAPSULE, GELATIN COATED in 1 BOTTLE (82804-304-60)

FDA lists these products with the same active ingredient.

69339-163 — LUBIPROSTONE, 70710-1641 — Lubiprostone, 70710-1642 — Lubiprostone, 70771-1763 — Lubiprostone, 70771-1764 — Lubiprostone, 71205-831 — lubiprostone, 71205-832 — lubiprostone, 71205-834 — Lubiprostone, 72189-410 — Lubiprostone, 72189-607 — Lubiprostone, 72603-288 — lubiprostone, 72603-289 — lubiprostone, 76420-777 — Lubiprostone, 76420-778 — Lubiprostone, 76420-906 — lubiprostone, 76420-907 — lubiprostone, 80425-0354 — lubiprostone, 80425-0355 — lubiprostone, 82804-001 — Lubiprostone, 83008-001 — 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.