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Lubiprostone

NDC 60687-827 · American Health Packaging

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

60687-827-32 — 20 BLISTER PACK in 1 CARTON (60687-827-32) / 1 CAPSULE, GELATIN COATED in 1 BLISTER PACK (60687-827-33)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

0480-4138 — Lubiprostone, 23635-508 — lubiprostone, 23635-524 — lubiprostone, 31722-403 — lubiprostone, 31722-404 — lubiprostone, 43598-163 — Lubiprostone, 43598-168 — Lubiprostone, 51407-744 — lubiprostone, 51407-745 — lubiprostone, 60687-816 — 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, 70771-1763 — Lubiprostone, 70771-1764 — 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.