NDC 82804-001 – Lubiprostone

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

Human Prescription Drug

Product NDC82804-001

Product details

Brand name
Lubiprostone
Generic name
Lubiprostone
Labeler
Proficient Rx LP
Dosage form
Capsule, Gelatin Coated
Route
Oral
Marketing category
NDA AUTHORIZED GENERIC · NDA021908
Marketed since
January 1, 2023
Listing expires
December 31, 2026
Pharmacologic class
Chloride Channel Activator

Active ingredients

Uses, dosage, side effects and warnings for Lubiprostone →

Package NDC codes (3)

Package NDCDescriptionSince
82804-001-3030 CAPSULE, GELATIN COATED in 1 BOTTLE (82804-001-30)Aug 24, 2023
82804-001-6060 CAPSULE, GELATIN COATED in 1 BOTTLE (82804-001-60)Aug 24, 2023
82804-001-9090 CAPSULE, GELATIN COATED in 1 BOTTLE (82804-001-90)Aug 24, 2023

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