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Last Updated: March 19, 2026

Details for New Drug Application (NDA): 218640

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NDA 218640 describes LUBIPROSTONE, which is a drug marketed by Amneal, Ascent Pharms Inc, Dr Reddys, Ph Health, Teva Pharms Usa Inc, and Zydus Pharms, and is included in six NDAs. It is available from eight suppliers. Additional details are available on the LUBIPROSTONE profile page.

The generic ingredient in LUBIPROSTONE is lubiprostone. There are ten drug master file entries for this compound. Nineteen suppliers are listed for this compound. Additional details are available on the lubiprostone profile page.

Summary for 218640

Tradename:	LUBIPROSTONE
Applicant:	Ascent Pharms Inc
Ingredient:	lubiprostone
Patents:	0

Pharmacology for NDA: 218640

Mechanism of Action	Chloride Channel Activators

Medical Subject Heading (MeSH) Categories for 218640

Chloride Channel Agonists

Suppliers and Packaging for NDA: 218640

Tradename	Generic Name	Dosage	NDA	Application Type	Supplier	National Drug Code	Package Code	Package
LUBIPROSTONE	lubiprostone	CAPSULE;ORAL	218640	ANDA	Camber Pharmaceuticals, Inc.	31722-403	31722-403-60	60 CAPSULE in 1 BOTTLE (31722-403-60)
LUBIPROSTONE	lubiprostone	CAPSULE;ORAL	218640	ANDA	Camber Pharmaceuticals, Inc.	31722-404	31722-404-60	60 CAPSULE in 1 BOTTLE (31722-404-60)

Profile for product number 001

Active Rx/OTC/Discontinued:	RX	Dosage:	CAPSULE;ORAL			Strength	8MCG
Approval Date:	Jan 2, 2025	TE:	AB	RLD:	No

Profile for product number 002

Active Rx/OTC/Discontinued:	RX	Dosage:	CAPSULE;ORAL			Strength	24MCG
Approval Date:	Jan 2, 2025	TE:	AB	RLD:	No

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