Lubiprostone
NDC 63304-352 · Sun Pharmaceutical Industries, 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
63304-352-60 — 60 CAPSULE, GELATIN COATED in 1 BOTTLE (63304-352-60)
Related Codes
Same active ingredient
FDA lists these products with the same active ingredient.
23635-524 — lubiprostone, 31722-403 — lubiprostone, 31722-404 — lubiprostone, 43598-163 — Lubiprostone, 43598-168 — Lubiprostone, 51407-744 — lubiprostone, 51407-745 — lubiprostone, 60687-816 — Lubiprostone, 60687-827 — Lubiprostone, 63304-351 — 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, 71205-831 — lubiprostone, 71205-832 — lubiprostone, +21 more