Strength
8 ug/1
Manufacturer
Sun Pharmaceutical Industries Inc.NDC
63304035160
Classification
Generic
Dosage Form
CAPSULE, GELATIN COATED
Route
ORAL
Last Updated
4/22/2026
Active Ingredients
LUBIPROSTONEApproval Type
Authorized Generic (NDA)
FDA Application
NDA021908On Market Since
1/1/2023
Pharmacological Classes
Chloride Channel Activator
Chloride Channel Activators
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