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Drug Product Composition: Potassium Chloride

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USFDA APPLICATION NUMBER - 213135 / DOSAGE - TABLET;ORAL - 0.225GM;0.188GM;1.479GM

Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
MAGNESIUM SULFATE ANHYDROUS(UNII: ML30MJ2U7I)
(MAGNESIUM CATION - UNII:T6V3LHY838)
MAGNESIUM SULFATE ANHYDROUS2.7g
POTASSIUM CHLORIDE(UNII: 660YQ98I10)
(POTASSIUM CATION - UNII:295O53K152)
POTASSIUM CATION2.25g
SODIUM SULFATE(UNII: 0YPR65R21J)
(SODIUM SULFATE ANHYDROUS - UNII:36KCS0R750)
SODIUM SULFATE17.75g

Inactive Ingredients

Ingredient Name
Braintree Laboratories, Inc.
ETHYLENE GLYCOL(FC72KVT52F)
POLYETHYLENE GLYCOL 8000(Q662QK8M3B)
POLYVINYL ALCOHOL GRAFT POLYETHYLENE GLYCOL COPOLYMER (3:1; 45000 MW)(23ZQ42JZZH)
SODIUM CAPRYLATE(9XTM81VK2B)