Strength
8 ug/1
Manufacturer
Teva Pharmaceuticals USA Inc.NDC
00480347906
Classification
Generic
Dosage Form
CAPSULE, GELATIN COATED
Route
ORAL
Last Updated
4/22/2026
Active Ingredients
LUBIPROSTONEApproval Type
Generic (ANDA)
FDA Application
ANDA209920On Market Since
1/3/2023
Pharmacological Classes
Chloride Channel Activator
Chloride Channel Activators
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