NDC 82804-304 – Lubiprostone

Lubiprostone 24 ug/1 · Capsule, Gelatin Coated · Oral

Human Prescription Drug

Product NDC82804-304

Product details

Brand name
Lubiprostone
Generic name
Lubiprostone
Labeler
Proficient Rx LP
Dosage form
Capsule, Gelatin Coated
Route
Oral
Marketing category
ANDA · ANDA209920
Marketed since
January 3, 2023
Listing expires
December 31, 2027
Pharmacologic class
Chloride Channel Activator

Active ingredients

Uses, dosage, side effects and warnings for Lubiprostone →

Package NDC codes (1)

Package NDCDescriptionSince
82804-304-6060 CAPSULE, GELATIN COATED in 1 BOTTLE (82804-304-60)Jul 21, 2026

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