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Drug Product Composition: Potassium Chloride

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USFDA APPLICATION NUMBER - 18279 / DOSAGE - TABLET, EXTENDED RELEASE;ORAL - 20MEQ **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
POTASSIUM CHLORIDE(UNII: 660YQ98I10)
(POTASSIUM CATION - UNII:295O53K152)
POTASSIUM CHLORIDE750mg

Inactive Ingredients

Ingredient Name
A-S Medication Solutions
American Health Packaging
Bryant Ranch Prepack
Lake Erie Medical DBA Quality Care Products LLC
Major Pharmaceuticals
Preferred Pharmaceuticals Inc.
Preferred Pharmaceuticals, Inc.
REMEDYREPACK INC.
St. Mary's Medical Park Pharmacy
REMEDYREPACK INC.
.ALPHA.-TOCOPHEROL(H4N855PNZ1) 
ALPHA-TOCOPHEROL(H4N855PNZ1)         
CASTOR OIL(D5340Y2I9G) 
COLLOIDAL SILICON DIOXIDE(ETJ7Z6XBU4)        
D&C YELLOW NO. 10(35SW5USQ3G)  
ETHYLCELLULOSE, UNSPECIFIED(7Z8S9VYZ4B)    
ETHYLCELLULOSES(7Z8S9VYZ4B)      
MAGNESIUM STEARATE(70097M6I30) 
PARAFFIN(I9O0E3H2ZE) 
POLYVINYL ACETATE(32K497ZK2U)   
SILICON DIOXIDE(ETJ7Z6XBU4)  
TITANIUM DIOXIDE(15FIX9V2JP) 
VANILLIN(CHI530446X)