Overview
Magnesium chloride salts are highly soluble in water and the hydrated form of magnesium chloride can be extracted from brine or sea water.
Indication
Magnesium chloride is used in several medical and topical (skin related) applications. Magnesium chloride usp, anhydrous uses as electrolyte replenisher, pharmaceutic necessity for hemodialysis and peritoneal dialysis fluids.
Associated Conditions
- Electrolyte imbalance
- Magnesium Deficiency
- Mild Metabolic acidosis
Clinical Trials
Title | Posted | Study ID | Phase | Status | Sponsor |
---|---|---|---|---|---|
2021/10/05 | Phase 1 | Completed | |||
2009/07/07 | Phase 2 | Completed |
FDA Drug Approvals
Approved Product | Manufacturer | NDC Code | Route | Strength | Effective Date |
---|---|---|---|---|---|
Baxter Healthcare Company | 0338-0210 | INTRAVENOUS | 51 mg in 100 mL | 9/21/2020 | |
Baxter Healthcare Corporation | 0338-0210 | INTRAVENOUS | 51 mg in 100 mL | 9/21/2020 | |
Fresenius Medical Care North America | 49230-212 | INTRAPERITONEAL | 5.08 mg in 100 mL | 10/19/2023 | |
Baxter Healthcare Corporation | 24571-111 | INTRAVENOUS | 3.05 g in 1 L | 11/1/2018 | |
ICU Medical Inc. | 0990-7372 | INTRAVENOUS | 30 mg in 100 mL | 3/8/2021 | |
Baxter Healthcare Company | 0338-1147 | INTRAVENOUS | 51 mg in 100 mL | 9/21/2020 | |
Baxter Healthcare Corporation | 0338-1147 | INTRAVENOUS | 51 mg in 100 mL | 9/21/2020 | |
Baxter Healthcare Company | 0338-1142 | INTRAVENOUS | 51 mg in 100 mL | 9/21/2020 | |
Baxter Healthcare Corporation | 0338-1142 | INTRAVENOUS | 51 mg in 100 mL | 9/21/2020 | |
Baxter Healthcare Corporation | 0941-0433 | INTRAPERITONEAL | 5.08 mg in 100 mL | 11/21/2019 |
EMA Drug Approvals
Approved Product | Authorization Holder | Status | Issued Date |
---|---|---|---|
No EMA approvals found for this drug. |
HSA Drug Approvals
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 | |
OLIMEL N9E EMULSION FOR INFUSION | N/A | N/A | N/A | 10/24/2013 | |
BALANCE 4.25% GLU. 1.25MMOL/L CAL. P.D. SOLUTION (JAPAN) | N/A | N/A | N/A | 7/12/2005 | |
PLASMA-LYTE 148 AND GLUCOSE 5% W/V SOLUTION FOR INFUSION | N/A | N/A | N/A | 8/23/2024 | |
VOLULYTE 6% SOLUTION FOR INFUSION | N/A | N/A | N/A | 7/20/2009 | |
CAPD/DPCA 18 PERITONEAL DIALYSIS SOLUTION | N/A | N/A | N/A | 5/13/2010 | |
PHYSIONEAL 40 DEXTROSE 1.5% P.D. SOLUTION | N/A | N/A | N/A | 10/10/2005 | |
DIANEAL LOW CALCIUM PERITONEAL SOLN 2.5% | N/A | N/A | N/A | 7/17/1991 | |
DIANEAL LOW CALCIUM P.D.SOLN & 1.5%DEXT | N/A | N/A | N/A | 3/12/1990 |
TGA Drug Approvals
Approved Product | ARTG ID | Sponsor | Registration Type | Status | Registration Date |
---|---|---|---|---|---|
SYNTHAMIN 17 Amino acid 10% with Electrolytes and Glucose 25% 1000mL injection AHB6350 | 19609 | Medicine | A | 9/30/1991 | |
SLEEP SAFE BALANCE 1.5% glucose 1.75 mmol/L calcium peritoneal dialysis solution bag | 92935 | Medicine | A | 6/20/2003 | |
METAGENICS ZINC DRINK | 64051 | Medicine | A | 4/27/1998 | |
OLICLINOMEL N4-550 E 1000 mL IV emulsion for infusion with electrolytes bag | 136599 | Medicine | A | 9/4/2007 | |
OLICLINOMEL N4-550 E 2500 mL IV emulsion for infusion with electrolytes bag | 141396 | Medicine | A | 9/4/2007 | |
HEMOSOL B0 haemofiltration / haemodiafiltration solution bag | 260992 | Medicine | A | 12/14/2016 | |
OLIMEL N5-860E Emulsion for intravenous infusion | 197417 | Medicine | A | 8/9/2013 | |
Caruso's Super Magnesium Cream | 310528 | Medicine | A | 10/19/2018 | |
TeenSleep and Stress | 380170 | Medicine | A | 12/3/2021 | |
MULTIBIC potassium-free, Solution for Haemofiltration | 357591 | Medicine | A | 8/2/2021 |
Health Canada Drug Approvals
Approved Product | Company | DIN | Dosage Form | Strength | Market Date |
---|---|---|---|---|---|
ACID CONCENTRATE RZ119C | genpharm ulc | N/A | Liquid - Haemodialysis | 3.431 G / L | 12/31/1995 |
ACID CONCENTRATE RO4137 | genpharm ulc | N/A | Liquid - Haemodialysis | 3.744 G / L | 12/31/1995 |
SELECTBAG ONE (AX 450 G) | Vantive ULC | 02415488 | Solution - Haemodialysis | 20.3 G / L | 4/21/2017 |
SB 1000 | renal systems, division of minntech corp. | 00678783 | Liquid - Haemodialysis | 3.7 G / L | 12/31/1985 |
PRISMASOL 2 | Vantive ULC | 02277441 | Solution - Intravenous
,
Haemodialysis | 2.033 G / L | 2/21/2006 |
PREMNIX HP | terra botanica products ltd. | 02233359 | Liquid - Oral | 30 X | 5/25/1998 |
ACID CONCENTRATE D12303 | althin biopharm inc. | 02217627 | Liquid - Haemodialysis | 1.61 G / L | 12/31/1996 |
ACID CONCENTRATE RZ254C | genpharm ulc | 02178389 | Liquid - Haemodialysis | 6.861 G / L | 12/31/1995 |
4.25% TRAVASOL AMINO ACID INJECTION WITH ELECTROLYTES IN 10% DEXTROSE | baxter corporation clintec nutrition division | N/A | Solution - Intravenous | 51 MG / 100 ML | 12/31/1996 |
ACID CONCENTRATE D-18003 | baxter corporation | 02158132 | Liquid - Haemodialysis | 2.5 G / L | 12/31/1995 |
CIMA AEMPS Drug Approvals
Approved Product | Company | Registration Number | Pharmaceutical Form | Prescription Type | Status |
---|---|---|---|---|---|
No CIMA AEMPS (Spain) approvals found for this drug. |
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. |
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