Lubiprostone

NDC 31722-404 · Camber Pharmaceuticals, Inc.

Generic namelubiprostone

Dosage formCAPSULE

RouteORAL

Active ingredient(s)LUBIPROSTONE

Strength.024 mg/1

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

Marketing categoryANDA

Packages

31722-404-60 — 60 CAPSULE in 1 BOTTLE (31722-404-60)

FDA lists these products with the same active ingredient.

0254-3028 — Lubiprostone, 0254-3029 — Lubiprostone, 0406-6408 — Lubiprostone, 0406-6424 — Lubiprostone, 0480-3479 — Lubiprostone, 0480-4138 — Lubiprostone, 23635-508 — lubiprostone, 23635-524 — lubiprostone, 31722-403 — lubiprostone, 43598-163 — Lubiprostone, 43598-168 — Lubiprostone, 51407-744 — lubiprostone, 51407-745 — lubiprostone, 60687-816 — Lubiprostone, 60687-827 — Lubiprostone, 63304-351 — lubiprostone, 63304-352 — lubiprostone, 64764-080 — lubiprostone, 64764-240 — lubiprostone, 69339-162 — 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.