NDC 31722-404 – Lubiprostone

Lubiprostone .024 mg/1 · Capsule · Oral

Human Prescription Drug

Product NDC31722-404

Product details

Brand name
Lubiprostone
Generic name
Lubiprostone
Labeler
Camber Pharmaceuticals, Inc.
Dosage form
Capsule
Route
Oral
Marketing category
ANDA · ANDA218640
Marketed since
May 27, 2025
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
31722-404-6060 CAPSULE in 1 BOTTLE (31722-404-60)May 27, 2025

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