Overview
Calcium chloride is an ionic compound of calcium and chlorine. It is highly soluble in water and it is deliquescent. It is a salt that is solid at room temperature, and it behaves as a typical ionic halide. It has several common applications such as brine for refrigeration plants, ice and dust control on roads, and in cement. It can be produced directly from limestone, but large amounts are also produced as a by-product of the Solvay process. Because of its hygroscopic nature, it must be kept in tightly-sealed containers.
Indication
For the treatment of hypocalcemia in those conditions requiring a prompt increase in blood plasma calcium levels, for the treatment of magnesium intoxication due to overdosage of magnesium sulfate, and used to combat the deleterious effects of hyperkalemia as measured by electrocardiographic (ECG), pending correction of the increased potassium level in the extracellular fluid.
Associated Conditions
- Acute Renal Failure (ARF)
- Dehydration
- Dehydration Hypertonic
- Dry Mouth
- Electrolyte depletion
- End-stage Chronic Kidney Failure
- Fluid Loss
- Hyperkalemia
- Hypocalcemia
- Hypocalcemic tetany
- Hypovolaemia
- Isotonic Dehydration
- Renal Failure, Chronic Renal Failure
- Shock, Hypovolemic
- Beta blocker overdose
- Calcium channel blocker overdose
Clinical Trials
Title | Posted | Study ID | Phase | Status | Sponsor |
---|---|---|---|---|---|
2024/04/22 | Phase 3 | Recruiting | |||
2023/08/03 | Early Phase 1 | Completed | |||
2022/12/23 | Phase 4 | Recruiting | |||
2022/07/01 | Phase 4 | UNKNOWN | Post Graduate Institute of Medical Education and Research, Chandigarh | ||
2021/09/16 | Phase 3 | UNKNOWN | |||
2021/08/30 | Phase 3 | Completed | |||
2020/01/18 | Phase 4 | Terminated | |||
2019/11/06 | Phase 2 | Completed | Lars Wiuff Andersen | ||
2019/03/08 | Phase 1 | Completed | |||
2018/12/12 | Phase 4 | Completed | Meshalkin Research Institute of Pathology of Circulation |
FDA Drug Approvals
Approved Product | Manufacturer | NDC Code | Route | Strength | Effective Date |
---|---|---|---|---|---|
Baxter Healthcare Company | 0338-0210 | INTRAVENOUS | 33 mg in 100 mL | 9/21/2020 | |
Baxter Healthcare Corporation | 0338-0210 | INTRAVENOUS | 33 mg in 100 mL | 9/21/2020 | |
Baxter Healthcare Corporation | 0338-0117 | INTRAVENOUS | 20 mg in 100 mL | 10/9/2019 | |
Medical Purchasing Solutions, LLC | 71872-7193 | INTRAVENOUS | 100 mg in 1 mL | 5/10/2023 | |
ICU Medical Inc. | 0990-7111 | INTRAVENOUS | 0.2 g in 1000 mL | 6/24/2021 | |
Fresenius Medical Care North America | 49230-212 | INTRAPERITONEAL | 18.4 mg in 100 mL | 10/19/2023 | |
Baxter Healthcare Corporation | 0338-0137 | IRRIGATION | 200 mg in 1000 mL | 9/29/2015 | |
Baxter Healthcare Company | 0338-1147 | INTRAVENOUS | 33 mg in 100 mL | 9/21/2020 | |
Baxter Healthcare Corporation | 0338-1147 | INTRAVENOUS | 33 mg in 100 mL | 9/21/2020 | |
Baxter Healthcare Company | 0338-1142 | INTRAVENOUS | 33 mg in 100 mL | 9/21/2020 |
EMA Drug Approvals
Approved Product | Authorization Holder | Status | Issued Date |
---|---|---|---|
No EMA approvals found for this drug. |
HSA Drug Approvals
Approved Product | Manufacturer | Approval Number | Dosage Form | Strength | Approval Date |
---|---|---|---|---|---|
COMPOUND SODIUM LACTATE INTRAVENOUS INFUSION BP | SIN06429P | INJECTION | 0.027 g/100 ml | 7/8/1991 | |
LACTATED RINGER'S INJECTION USP | SIN05592P | INJECTION | 20 mg/100 ml | 3/27/1991 | |
BAXTER-LACTATED RINGER’S INJECTION USP | SIN16604P | INFUSION, SOLUTION | 20mg per 100mL | 9/14/2022 | |
HAEMODIALYSIS CONCENTRATE NKFS-01 (ACID) FOR BICARBONATE DIALYSIS | SIN09474P | SOLUTION | 7.77 g/l | 8/21/1997 | |
TISSEEL FIBRIN SEALANT VH S/D (FROZEN) | SIN14707P | SOLUTION | 36-44 umol/ml | 12/22/2014 | |
BERIPLAST P COMBI-SET 3ML POWDERS AND SOLVENTS FOR SEALANT | SIN16776P | OTHER | 17.7mg | 5/10/2023 | |
LACTORIDE 500 INFUSION | SIN09647P | INJECTION | 0.027% w/v | 2/18/1998 | |
ARTISS SOLUTIONS FOR SEALANT, DEEP FROZEN | SIN14719P | SOLUTION | 36 – 44 μmol/ml | 1/6/2015 | |
BERIPLAST P COMBI-SET 1ML POWDERS AND SOLVENTS FOR SEALANT | SIN16775P | OTHER | 5.9mg | 5/10/2023 | |
DIANEAL LOW CALCIUM (2.5 mEq/l) PERITONEAL DIALYSIS SOLUTION WITH 1.5% DEXTROSE | SIN06627P | SOLUTION, STERILE | 18.3 mg/100 ml | 10/14/1991 |
NMPA Drug Approvals
Approved Product | Company | Approval Number | Drug Type | Dosage Form | Approval Date |
---|---|---|---|---|---|
No NMPA approvals found for this drug. |
PPB Drug Approvals
Approved Product | Registration No. | Company | Licence No. | Strength | Registration Date |
---|---|---|---|---|---|
EXTRANEAL SOLN 7.5% | N/A | N/A | N/A | 8/18/2000 | |
PRISMASOL B0 SOLUTION FOR HAEMOFILTRATION AND HAEMODIALYSIS | N/A | N/A | N/A | 10/15/2013 | |
RINGER'S INJ | N/A | otsuka pharmaceutical (h.k.) limited | N/A | N/A | 5/15/2008 |
LACTATED RINGER'S INJ | N/A | N/A | N/A | 5/17/1979 | |
OLIMEL N9E EMULSION FOR INFUSION | N/A | N/A | N/A | 10/24/2013 | |
NUTRIFLEX OMEGA SPECIAL EMULSION FOR INFUSION | N/A | N/A | N/A | 1/11/2012 | |
BALANCE 4.25% GLU. 1.25MMOL/L CAL. P.D. SOLUTION (JAPAN) | N/A | N/A | N/A | 7/12/2005 | |
WIDA RL RINGER LACTATE INTRAVENOUS INFUSION | N/A | otsuka pharmaceutical (h.k.) limited | N/A | N/A | 10/30/2009 |
SMOFKABIVEN EMULSION FOR INFUSION | N/A | N/A | N/A | 5/26/2011 | |
NAMIDA EYE-RUBY EYE DROPS | N/A | eng an trading company limited | N/A | N/A | 5/7/1996 |
TGA Drug Approvals
Health Canada Drug Approvals
Approved Product | Company | DIN | Dosage Form | Strength | Market Date |
---|---|---|---|---|---|
ACID CONCENTRATE RZ119C | genpharm ulc | N/A | Liquid - Haemodialysis | 9.924 G / L | 12/31/1995 |
ACID CONCENTRATE RO4137 | genpharm ulc | N/A | Liquid - Haemodialysis | 6.769 G / L | 12/31/1995 |
SB 1000 | renal systems, division of minntech corp. | 00678783 | Liquid - Haemodialysis | 9.5 G / L | 12/31/1985 |
SELECTBAG ONE (AX 450 G) | Vantive ULC | 02415488 | Solution - Haemodialysis | 44.1 G / L | 4/21/2017 |
PRISMASOL 2 | Vantive ULC | 02277441 | Solution - Intravenous
,
Haemodialysis | 5.145 G / L | 2/21/2006 |
ACID CONCENTRATE D-18003 | baxter corporation | 02158132 | Liquid - Haemodialysis | 4.85 G / L | 12/31/1995 |
ACID CONCENTRATE RZ254C | genpharm ulc | 02178389 | Liquid - Haemodialysis | 8.27 G / L | 12/31/1995 |
ACID CONCENTRATE D12303 | althin biopharm inc. | 02217627 | Liquid - Haemodialysis | 8.78 G / L | 12/31/1996 |
CALCIUM CHLORIDE BP - ADDITIVE FOR CONCENTRATED HAEMODIALYSIS SOLUTIONS | genpharm ulc | 02230676 | Powder - Haemodialysis | 12.32 G / VIAL | 6/18/1998 |
FORMULA 22158 | therapeutic foods co. | 00191531 | Capsule - Oral | 7 MG / CAP | 5/18/1994 |
CIMA AEMPS Drug Approvals
Approved Product | Company | Registration Number | Pharmaceutical Form | Prescription Type | Status |
---|---|---|---|---|---|
CELSIOR SOLUCION PARA LA CONSERVACION DE ORGANOS | Institut Georges Lopez | 73767 | SOLUCIÓN PARA CONSERVACIÓN DE ÓRGANOS | Uso Hospitalario | Commercialized |
BICAVERA GLUCOSA 1,5%, Calcio 1,75 mmol/l SOLUCION PARA DIALISIS PERITONEAL | 64755 | SOLUCION PARA DIALISIS PERITONEAL | Uso Hospitalario | Commercialized | |
TISSEEL SOLUCIONES PARA ADHESIVO TISULAR | Baxter S.L. | 78896 | SOLUCIÓN PARA ADHESIVO TISULAR | Uso Hospitalario | Commercialized |
KABIPAC SOLUCION RINGER SOLUCIÓN PARA PERFUSIÓN | Fresenius Kabi España, S.A.U. | 60265 | SOLUCIÓN PARA PERFUSIÓN | Medicamento Sujeto A Prescripción Médica | Commercialized |
MULTIBIC 3 MMOL/L DE POTASIO SOLUCIÓN PARA HEMODIÁLISIS Y HEMOFILTRACIÓN | 65814 | SOLUCIÓN PARA HEMOFILTRACIÓN | Medicamento Sujeto A Prescripción Médica | Commercialized | |
MULTIBIC 4 MMOL/L DE POTASIO SOLUCIÓN PARA HEMODIÁLISIS Y HEMOFILTRACIÓN | 65815 | SOLUCIÓN PARA HEMOFILTRACIÓN | Medicamento Sujeto A Prescripción Médica | Commercialized | |
KABIVEN EMULSION PARA PERFUSION | 62985 | EMULSIÓN PARA PERFUSIÓN | Uso Hospitalario | Commercialized | |
PRISMASOL 2 mmol/l POTASIO, SOLUCION PARA HEMODIALISIS Y HEMOFILTRACION | Vantive Belgium | 65896 | SOLUCIÓN PARA HEMOFILTRACIÓN | Uso Hospitalario | Commercialized |
KABIVEN PERIFERICO EMULSION PARA PERFUSION | 63596 | EMULSIÓN PARA PERFUSIÓN | Uso Hospitalario | Not Commercialized | |
CLORURO DE CALCIO BRAUN 100 mg/ml SOLUCION INYECTABLE | B Braun Medical S.A. | 49072 | SOLUCIÓN INYECTABLE | Medicamento Sujeto A Prescripción Médica | Commercialized |
Philippines FDA Drug Approvals
Approved Product | Company | License Number | Dosage Form | Strength | Approval Date |
---|---|---|---|---|---|
No Philippines FDA approvals found for this drug. |
Saudi SFDA Drug Approvals
Approved Product | Company | License Number | Dosage Form | Strength | Approval Date |
---|---|---|---|---|---|
No Saudi SFDA approvals found for this drug. |
Malaysia NPRA Drug Approvals
Approved Product | Company | Registration Number | Dosage Form | Strength | Approval Date |
---|---|---|---|---|---|
No Malaysia NPRA approvals found for this drug. |
UK EMC Drug Information
Medicine Name | MA Holder | MA Number | Pharmaceutical Form | Active Ingredient | Authorization Date |
---|---|---|---|---|---|
No UK EMC drug information found for this drug. |
Help Us Improve
Your feedback helps us provide better drug information and insights.