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Drug Product Composition: Potassium Chloride

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USFDA APPLICATION NUMBER - 19685 / DOSAGE - INJECTABLE;INJECTION - 20MG/100ML;5GM/100ML;254MG/100ML;600MG/100ML;310MG/100ML

Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
CALCIUM CHLORIDE(UNII: M4I0D6VV5M)
(CHLORIDE ION - UNII:Q32ZN48698)
CALCIUM CHLORIDE0.2g in 1 | 0.2g in 1000
DEXTROSE MONOHYDRATE(UNII: LX22YL083G)
(ANHYDROUS DEXTROSE - UNII:5SL0G7R0OK)
DEXTROSE MONOHYDRATE50g in 1 | 50g in 1000
POTASSIUM CHLORIDE(UNII: 660YQ98I10)
(CHLORIDE ION - UNII:Q32ZN48698)
POTASSIUM CHLORIDE3.28g in 1 | 1.79g in 1000
SODIUM CHLORIDE(UNII: 451W47IQ8X)
(CHLORIDE ION - UNII:Q32ZN48698)
SODIUM CHLORIDE6g in 1 | 6g in 1000
SODIUM LACTATE(UNII: TU7HW0W0QT)
(LACTIC ACID, UNSPECIFIED FORM - UNII:33X04XA5AT)
SODIUM LACTATE3.1g in 1 | 3.1g in 1000

Inactive Ingredients

Ingredient Name
Hospira, Inc.
WATER(059QF0KO0R)