Strength
10 g/10g
Manufacturer
Cumberland Pharmaceuticals Inc.NDC
66220071930
Classification
Brand (ANDA)
Dosage Form
POWDER, FOR SOLUTION
Route
ORAL
Last Updated
1/1/2026
Active Ingredients
LACTULOSEApproval Type
Generic (ANDA)
FDA Application
ANDA074712On Market Since
1/20/2012
Pharmacological Classes
Acidifying Activity
Osmotic Activity
Osmotic Laxative
Stimulation Large Intestine Fluid/Electrolyte Secretion
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