NDC 72189-410 – Amitza

Lubiprostone 8 ug/1 · Capsule, Gelatin Coated · Oral

Human Prescription Drug

Product NDC72189-410

Product details

Brand name
Amitza
Generic name
Lubiprostone
Labeler
Direct_Rx
Dosage form
Capsule, Gelatin Coated
Route
Oral
Marketing category
ANDA · ANDA209920
Marketed since
January 12, 2023
Listing expires
December 31, 2026
Pharmacologic class
Chloride Channel Activator

Active ingredients

Uses, dosage, side effects and warnings for Amitza →

Package NDC codes (1)

Package NDCDescriptionSince
72189-410-6060 CAPSULE, GELATIN COATED in 1 BOTTLE (72189-410-60)Jan 12, 2023