Strength
1500 mg/1
Manufacturer
Upsher-Smith Laboratories LLCNDC
00245531990
Classification
Brand (ANDA)
Dosage Form
TABLET, EXTENDED RELEASE
Route
ORAL
Last Updated
4/22/2026
Active Ingredients
POTASSIUM CHLORIDEApproval Type
Generic (ANDA)
FDA Application
ANDA074726On Market Since
1/18/2011
Pharmacological Classes
Increased Large Intestinal Motility
Inhibition Large Intestine Fluid/Electrolyte Absorption
Osmotic Activity
Osmotic Laxative
Potassium Compounds
Potassium Salt
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