NDC 65162-841 – Lubiprostone

Lubiprostone 8 ug/1 · Capsule · Oral

Human Prescription Drug

Product NDC65162-841

Product details

Brand name
Lubiprostone
Generic name
Lubiprostone
Labeler
Amneal Pharmaceuticals LLC
Dosage form
Capsule
Route
Oral
Marketing category
ANDA · ANDA209450
Marketed since
December 3, 2021
Listing expires
December 31, 2027
Pharmacologic class
Chloride Channel Activator

Active ingredients

Uses, dosage, side effects and warnings for Lubiprostone →

Package NDC codes (2)

Package NDCDescriptionSince
65162-841-0660 CAPSULE in 1 BOTTLE (65162-841-06)Dec 3, 2021
65162-841-18180 CAPSULE in 1 BOTTLE (65162-841-18)Dec 3, 2021

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