NDC 0254-3029 – Lubiprostone

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

Human Prescription Drug

Product NDC0254-3029

Product details

Brand name
Lubiprostone
Generic name
Lubiprostone
Labeler
Par Health USA, LLC
Dosage form
Capsule, Gelatin Coated
Route
Oral
Marketing category
NDA AUTHORIZED GENERIC · NDA021908
Marketed since
January 1, 2021
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
0254-3029-0260 CAPSULE, GELATIN COATED in 1 BOTTLE (0254-3029-02)Jan 1, 2021

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