NDC 51407-744 – Lubiprostone

Lubiprostone 8 ug/1 · Capsule, Gelatin Coated · Oral

Human Prescription Drug

Product NDC51407-744

Product details

Brand name
Lubiprostone
Generic name
Lubiprostone
Labeler
Golden State Medical Supply, Inc.
Dosage form
Capsule, Gelatin Coated
Route
Oral
Marketing category
NDA AUTHORIZED GENERIC · NDA021908
Marketed since
April 29, 2008
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
51407-744-6060 CAPSULE, GELATIN COATED in 1 BOTTLE (51407-744-60)Jan 23, 2023

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