Lubiprostone (lubiprostone)

**Product type:** Human Prescription Drug

**Active ingredient:** LUBIPROSTONE

**Strength:** 8 ug/1

**Dosage form:** Capsule, Gelatin Coated

**Route:** Oral

**Labeler:** Sun Pharmaceutical Industries, Inc.

**Marketing category:** NDA AUTHORIZED GENERIC (NDA021908)

**Pharmacologic class:** Chloride Channel Activator [EPC], Chloride Channel Activators [MoA]