LUBIPROSTONE

NDC 69339-163 · Natco Pharma USA LLC

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

69339-163-17 — 40 BLISTER PACK in 1 CARTON (69339-163-17) / 1 CAPSULE, GELATIN COATED in 1 BLISTER PACK (69339-163-98)

FDA lists these products with the same active ingredient.

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, 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, +21 more

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