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USFDA APPLICATION NUMBER - 16682 / DOSAGE - INJECTABLE;INJECTION - 20MG/100ML;30MG/100ML;600MG/100ML;310MG/100ML
| Active Ingredient/Active Moiety | ||
| Ingredient Name | Basis of Strength | Strength |
|---|---|---|
| CALCIUM CHLORIDE(UNII: M4I0D6VV5M) (CALCIUM CATION - UNII:2M83C4R6ZB) | CALCIUM CHLORIDE | 20mg in 100 |
| POTASSIUM CHLORIDE(UNII: 660YQ98I10) (POTASSIUM CATION - UNII:295O53K152) | POTASSIUM CHLORIDE | 30mg in 100 |
| SODIUM CHLORIDE(UNII: 451W47IQ8X) (CHLORIDE ION - UNII:Q32ZN48698) | SODIUM CHLORIDE | 600mg in 100 |
| SODIUM LACTATE(UNII: TU7HW0W0QT) (LACTIC ACID - UNII:33X04XA5AT) | SODIUM LACTATE | 310mg in 100 |
Inactive Ingredients
| Ingredient Name | Hospira, Inc. | B. Braun Medical Inc. | Baxter Healthcare Corporation | REMEDYREPACK INC. |
|---|---|---|---|---|
| HYDROCHLORIC ACID(QTT17582CB) | ||||
| SODIUM HYDROXIDE(55X04QC32I) | ||||
| WATER(059QF0KO0R) |
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