NDC 80425-0355 – Lubiprostone

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

Human Prescription Drug

Product NDC80425-0355

Product details

Brand name
Lubiprostone
Generic name
Lubiprostone
Labeler
Advanced Rx of Tennessee, LLC
Dosage form
Capsule, Gelatin Coated
Route
Oral
Marketing category
NDA AUTHORIZED GENERIC · NDA021908
Marketed since
August 16, 2023
Listing expires
December 31, 2026
Pharmacologic class
Chloride Channel Activator

Active ingredients

Uses, dosage, side effects and warnings for Lubiprostone →

Package NDC codes (1)

Package NDCDescriptionSince
80425-0355-260 CAPSULE, GELATIN COATED in 1 BOTTLE (80425-0355-2)Aug 16, 2023

Other Lubiprostone products