NDC 76420-778 – Lubiprostone

Lubiprostone 24 ug/1 · Capsule · Oral

Human Prescription Drug

Product NDC76420-778

Product details

Brand name
Lubiprostone
Generic name
Lubiprostone
Labeler
Asclemed 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 (4)

Package NDCDescriptionSince
76420-778-01100 CAPSULE in 1 BOTTLE (76420-778-01)Feb 7, 2025
76420-778-3030 CAPSULE in 1 BOTTLE (76420-778-30)Feb 7, 2025
76420-778-6060 CAPSULE in 1 BOTTLE (76420-778-60)Feb 7, 2025
76420-778-9090 CAPSULE in 1 BOTTLE (76420-778-90)Feb 7, 2025

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