USFDA APPLICATION NUMBER - 19691 / DOSAGE - INJECTABLE;INJECTION - 5GM/100ML;298MG/100ML;900MG/100ML
Active Ingredient/Active Moiety | ||
Ingredient Name | Basis of Strength | Strength |
---|---|---|
DEXTROSE MONOHYDRATE(UNII: LX22YL083G) (ANHYDROUS DEXTROSE - UNII:5SL0G7R0OK) | DEXTROSE MONOHYDRATE | 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 | 50g in 1000 |
POTASSIUM CHLORIDE(UNII: 660YQ98I10) (CHLORIDE ION - UNII:Q32ZN48698) | POTASSIUM CHLORIDE | 0.745g 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 CHLORIDE | 2.25g 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) |
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