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Drug Product Composition: Potassium Chloride

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USFDA APPLICATION NUMBER - 19691 / DOSAGE - INJECTABLE;INJECTION - 5GM/100ML;74.5MG/100ML;900MG/100ML

Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
DEXTROSE MONOHYDRATE(UNII: LX22YL083G)
(ANHYDROUS DEXTROSE - UNII:5SL0G7R0OK)
DEXTROSE MONOHYDRATE50g in 1000 | 50g in 1000 | 50g in 1000 | 50g in 1000 | 50g in 1000 | 50g in 1000 | 50g in 1000 | 50g in 1000 | 50g in 1000 | 50g in 1000 | 50g in 1000
POTASSIUM CHLORIDE(UNII: 660YQ98I10)
(CHLORIDE ION - UNII:Q32ZN48698)
POTASSIUM CHLORIDE0.745g in 1000 | 1.49g in 1000 | 1.49g in 1000 | 1.49g in 1000 | 0.745g in 1000 | 2.98g in 1000 | 2.24g in 1000 | 2.98g in 1000 | 2.24g in 1000 | 2.98g in 1000 | 1.49g in 1000
SODIUM CHLORIDE(UNII: 451W47IQ8X)
(CHLORIDE ION - UNII:Q32ZN48698)
SODIUM CHLORIDE2.25g in 1000 | 4.5g in 1000 | 3g in 1000 | 2.25g in 1000 | 4.5g in 1000 | 2.25g in 1000 | 2.25g in 1000 | 4.5g in 1000 | 4.5g in 1000 | 9g in 1000 | 9g in 1000

Inactive Ingredients

Ingredient Name
Hospira, Inc.
HYDROCHLORIC ACID(QTT17582CB)
WATER(059QF0KO0R)