Strength
600 mg/1
Manufacturer
Upsher-Smith Laboratories LLCNDC
00245531501
Classification
Brand
Dosage Form
TABLET, FILM COATED, EXTENDED RELEASE
Route
ORAL
Last Updated
2/18/2026
Active Ingredients
POTASSIUM CHLORIDEApproval Type
New Drug (NDA)
FDA Application
NDA019123On Market Since
4/17/1986
Pharmacological Classes
Increased Large Intestinal Motility
Inhibition Large Intestine Fluid/Electrolyte Absorption
Osmotic Activity
Osmotic Laxative
Potassium Compounds
Potassium Salt
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