NDC 60687-827 – Lubiprostone

Lubiprostone 24 ug/1 · Capsule, Gelatin Coated · Oral

Human Prescription Drug

Product NDC60687-827

Product details

Brand name
Lubiprostone
Generic name
Lubiprostone
Labeler
American Health Packaging
Dosage form
Capsule, Gelatin Coated
Route
Oral
Marketing category
ANDA · ANDA209920
Marketed since
November 26, 2025
Listing expires
December 31, 2027
Pharmacologic class
Chloride Channel Activator

Active ingredients

Uses, dosage, side effects and warnings for Lubiprostone →

Package NDC codes (1)

Package NDCDescriptionSince
60687-827-3220 BLISTER PACK in 1 CARTON (60687-827-32) / 1 CAPSULE, GELATIN COATED in 1 BLISTER PACK (60687-827-33)Nov 26, 2025

Other Lubiprostone products