NDC 71205-834 – Lubiprostone

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

Human Prescription Drug

Product NDC71205-834

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 (10)

Package NDCDescriptionSince
71205-834-00100 CAPSULE, GELATIN COATED in 1 BOTTLE (71205-834-00)Aug 18, 2023
71205-834-111000 CAPSULE, GELATIN COATED in 1 BOTTLE (71205-834-11)Aug 18, 2023
71205-834-3030 CAPSULE, GELATIN COATED in 1 BOTTLE (71205-834-30)Aug 18, 2023
71205-834-55500 CAPSULE, GELATIN COATED in 1 BOTTLE (71205-834-55)Aug 18, 2023
71205-834-6060 CAPSULE, GELATIN COATED in 1 BOTTLE (71205-834-60)Aug 18, 2023
71205-834-64240 CAPSULE, GELATIN COATED in 1 BOTTLE (71205-834-64)Aug 18, 2023
71205-834-67270 CAPSULE, GELATIN COATED in 1 BOTTLE (71205-834-67)Aug 18, 2023
71205-834-72120 CAPSULE, GELATIN COATED in 1 BOTTLE (71205-834-72)Aug 18, 2023
71205-834-78180 CAPSULE, GELATIN COATED in 1 BOTTLE (71205-834-78)Aug 18, 2023
71205-834-9090 CAPSULE, GELATIN COATED in 1 BOTTLE (71205-834-90)Aug 18, 2023

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