NDC 0406-6408 – Lubiprostone

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

Human Prescription Drug

Product NDC0406-6408

Product details

Brand name
Lubiprostone
Generic name
Lubiprostone
Labeler
SpecGx LLC
Dosage form
Capsule, Gelatin Coated
Route
Oral
Marketing category
NDA AUTHORIZED GENERIC · NDA021908
Marketed since
May 1, 2024
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
0406-6408-6060 CAPSULE, GELATIN COATED in 1 BOTTLE (0406-6408-60)May 1, 2024

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