NDC 70710-1642 – Lubiprostone

Lubiprostone 24 ug/1 · Capsule · Oral

Human Prescription Drug

Product NDC70710-1642

Product details

Brand name
Lubiprostone
Generic name
Lubiprostone
Labeler
Zydus Pharmaceuticals USA Inc.
Dosage form
Capsule
Route
Oral
Marketing category
ANDA · ANDA214131
Marketed since
March 23, 2023
Listing expires
December 31, 2026
Pharmacologic class
Chloride Channel Activator

Active ingredients

Uses, dosage, side effects and warnings for Lubiprostone →

Package NDC codes (2)

Package NDCDescriptionSince
70710-1642-1100 CAPSULE in 1 BOTTLE (70710-1642-1)Mar 23, 2023
70710-1642-660 CAPSULE in 1 BOTTLE (70710-1642-6)Mar 23, 2023

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