CALCIUM CHLORIDE injection, solution

calcium chloride by

Drug Labeling and Warnings

calcium chloride by is a Prescription medication manufactured, distributed, or labeled by Amneal Pharmaceuticals LLC, Amneal Pharmaceuticals Private Limited. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

  • 1 INDICATIONS AND USAGE

    Calcium chloride injection is indicated for the treatment of adult and pediatric patients with acute symptomatic hypocalcemia.

    Limitations of Use

    The safety and effectiveness of calcium chloride injection for long-term use has not been established.

  • 2 DOSAGE AND ADMINISTRATION

    2.1 Important Administration Instructions

    Administer calcium chloride injection by slow intravenous infusion in a central or deep vein in adults and pediatric patients (with or without renal impairment); do not administer by bolus [see Warnings and Precautions (5.2, 5.4)]. The maximum recommended infusion rate is 1 mL/minute (100 mg/minute).

    Additional important administration instructions regarding calcium chloride injection are as follows:

    • Do not use intramuscularly or subcutaneously to avoid tissue necrosis calcinosis cutis [see Warnings and Precautions (5.4)].
    • Visually inspect for particulate matter and discoloration prior to administration (the solution is clear and the seal is intact). Do not administer if the solution is unclear or the seal is not intact.
    • Stop the administration if the patient complains of any administration-related discomfort; administration may be resumed when symptoms disappear.
    • Discard the unused portion.
    • If time permits, allow the solution to warm to body temperature.

    2.2 Recommended Dosage and Administration

    The recommended dose range of calcium chloride injection in:

    • Adults is from 200 mg to 1,000 mg.
    • Pediatric patients is from 2.7 mg/kg to 5 mg/kg of calcium chloride.

    Dosing of this calcium chloride injection product is not possible in patients who require doses less than 200 mg because the recommended dose cannot be achieved with the supplied syringe. For patients who require doses less than 200 mg, use another calcium chloride injection product that allows dosing of less than 200 mg.

    Individualize the dose for a patient within these dose ranges depending on serum ionized calcium level, severity of hypocalcemia symptoms and the acuity of hypocalcemia onset.

    Repeated injections may be required because of rapid excretion of calcium.

    2.3 Recommended Starting Dose in Patients with Renal Impairment

    The recommended starting dose of calcium chloride injection in [see Use in Specific Populations (8.6)]:

    • Adults with renal impairment is 200 mg.
    • Pediatric patients is 2.7 mg/kg of calcium chloride.

    2.4 Drug Incompatibilities

    Do not mix calcium chloride injection with other drugs simultaneously. Do not mix calcium chloride injection with ceftriaxone or administer these products simultaneously via a Y-site because concurrent use can lead to the formation of ceftriaxone-calcium precipitates [see Warnings and Precautions (5.1)]:

    • In neonates (28 days of age or younger), concomitant use of calcium chloride injection and ceftriaxone is contraindicated [see Contraindications (4)].
    • In patients older than 28 days of age, ceftriaxone and calcium-containing products may be administered sequentially, provided the infusion lines are thoroughly flushed between infusions with a compatible fluid.
  • 3 DOSAGE FORMS AND STRENGTHS

    Calcium Chloride Injection, USP (single-dose) supplied as:

    • 10% (1,000 mg/10 mL) (100 mg/mL) in a Vial
    • 10% (1,000 mg/10 mL) (100 mg/mL) in a Pre-Filled Glass Syringe

    The 100 mg/mL concentration represents 27 mg or 1.4 mEq of elemental calcium per mL of solution.

  • 4 CONTRAINDICATIONS

    Calcium chloride injection is contraindicated in:

    • Patients with ventricular fibrillation
    • Patients with asystole and electromechanical dissociation

    Newborns (up to 28 days of age) if they require (or are expected to require) ceftriaxone intravenous treatment because of the risk of precipitation of ceftriaxone-calcium, regardless of whether these products would be received at different times or through separate intravenous lines [see Warnings and Precautions (5.1)].

  • 5 WARNINGS AND PRECAUTIONS

    5.1 End-Organ Damage due to Intravascular Ceftriaxone-Calcium Precipitates

    The use of calcium chloride injection is contraindicated in newborns (up to 28 days of age) if they require (or are expected to require) ceftriaxone intravenous treatment because of the risk of precipitation of ceftriaxone-calcium, regardless of whether these products would be received at different times or through separate intravenous lines [see Contraindications (4)]. Cases of fatal reactions with calcium-ceftriaxone precipitates in lungs and kidneys in premature and full-term newborns aged less than 1 month have occurred when ceftriaxone and calcium were administered either simultaneously or non-simultaneously and through different intravenous lines. In-vitro studies demonstrated that neonates have an increased risk of precipitation of ceftriaxone-calcium compared to other age groups.

    In patients older than 28 days of age, calcium chloride injection and ceftriaxone intravenous solutions may be administered sequentially one after another if infusion lines at different sites are used, infusion lines are replaced, or infusion lines are thoroughly flushed between infusions with physiological salt solution to avoid precipitation. Do not mix or administer calcium chloride injection simultaneously with ceftriaxone, even if using different infusion lines or different infusion sites as it can lead to precipitation of ceftriaxone-calcium [see Dosage and Administration (2.4)].

    5.2 Hypotension, Bradycardia, Arrhythmias and Syncope with Rapid Administration

    Rapid injection of calcium chloride injection may cause vasodilation, decreased blood pressure, bradycardia, arrhythmias, syncope and cardiac arrest. It is particularly important to prevent a high concentration of calcium from reaching the heart because of the risk of syncope. Too rapid an injection exceeding 1 mL/minute may lead to hypotension and cardiac syncope [see Dosage and Administration (2.1)].

    5.3 Arrhythmias with Concomitant Digoxin Use

    Arrhythmias may occur if calcium chloride injection and digoxin are administered together. Hypercalcemia resulting from an overdose of calcium chloride injection increases the risk of digoxin toxicity. Avoid the use of calcium chloride injection in patients receiving digoxin. If concomitant therapy is necessary, closely monitor ECG and calcium levels [see Drug Interactions (7.1)].

    5.4 Tissue Necrosis and Calcinosis

    Administration of calcium chloride injection in patients with local trauma may result in calcinosis cutis due to transient increase in local calcium concentration. Calcinosis cutis can occur with or without extravasation of calcium chloride injection, is characterized by abnormal dermal deposits of calcium salts and clinically manifests as papules, plaques, or nodules that may be associated with erythema, swelling, or induration. Tissue necrosis, ulceration and secondary infection are the most serious complications.

    To minimize the risk of tissue necrosis, ulceration and calcinosis, administer calcium chloride injection slowly through a small needle into a large vein [see Dosage and Administration (2.1)]. Avoid extravasation or accidental injection into perivascular tissues. Should perivascular infiltration occur, immediately discontinue intravenous administration at that site and treat as needed.

    5.5 Aluminum Toxicity

    Calcium chloride injection contains aluminum that may be toxic. Aluminum may reach toxic levels with prolonged parenteral administration if kidney function is impaired. Premature neonates are particularly at risk because their kidneys are immature and they require large amounts of calcium and phosphate solutions, which contain aluminum. Research indicates that patients with impaired kidney function, including premature (preterm) neonates and preterm infants, who receive parenteral levels of aluminum at greater than 4 to 5 mcg/kg/day can accumulate aluminum at levels associated with central nervous system and bone toxicity. Tissue loading may occur at even lower amounts of aluminum.

    Exposure to aluminum from calcium chloride injection at the recommended dose is not more than 10 mcg [see Dosage and Administration (2.2) and Description (11)]. When prescribing calcium chloride injection in patients receiving parenteral nutrition solutions, limit the total daily patient exposure to aluminum to no more than 5 mcg/kg/day.

  • 6 ADVERSE REACTIONS

    The following serious adverse reactions are also described elsewhere in the labeling:

    The following adverse reactions have been identified in literature and post-marketing reports of calcium chloride. Because some of these reactions were reported voluntarily from a population of uncertain size, it is not always possible to reliably estimate their frequency or establish a causal relationship to drug exposure:

    • Nervous system disorders: Paraesthesia (upon rapid injection), calcium taste
    • General disorders and administration site conditions: Sense of oppression, sense of “heat wave”, local burning sensation, injection site extravasation, injection site reactions
    • Cardiovascular disorders: Peripheral vasodilation, decreased blood pressure
  • 7 DRUG INTERACTIONS

    7.1 Digoxin

    Avoid the concomitant use of calcium chloride injection with digoxin. If concomitant use is unavoidable, monitor ECG closely during administration of calcium chloride injection.

    Synergistic arrhythmias may occur with concomitant use. The use of calcium chloride injection may result in hypercalcemia which increases the risk of digoxin toxicity [see Warnings and Precautions (5.3)].

    7.2 Calcium Channel Blockers

    Concomitant use of calcium chloride injection and calcium channel blockers may reduce the response to calcium channel blockers. Avoid concomitant use. If concomitant use is unavoidable, monitor blood pressure closely during administration of calcium chloride injection.

    7.3 Drugs That Increase the Risk of Hypercalcemia

    Increase frequency of monitoring of calcium concentrations in patients taking concomitant calcium chloride injection and other drugs that increase the risk of hypercalcemia (e.g., calcipotriene, estrogen, lithium, parathyroid hormone, teriparatide, thiazide diuretics, Vitamin A and Vitamin D).

  • 8 USE IN SPECIFIC POPULATIONS

    8.1 Pregnancy

    Risk Summary

    Administration of calcium chloride injection for the treatment of acute symptomatic hypocalcemia during pregnancy is not expected to cause major birth defects, miscarriage, or adverse maternal or fetal outcomes. There are risks to the mother and the fetus associated with development of hypocalcemia during pregnancy (see Clinical Considerations). Animal reproduction studies have not been conducted with calcium chloride injection.

    The estimated background risk of major birth defects and miscarriage for the indicated populations are unknown. All pregnancies have a background risk of birth defect, loss, or other adverse outcomes. In the U.S. general population, the estimated background risk of major birth defects and miscarriage in clinically recognized pregnancies is 2% to 4% and 15% to 20%, respectively.

    Clinical Considerations

    Disease-associated Maternal and/or Embryo/Fetal/Neonatal Risk

    Maternal hypocalcemia can result in an increased rate of spontaneous abortion, premature and dysfunctional labor and possibly preeclampsia. Infants born to mothers with hypocalcemia can develop fetal and neonatal hyperparathyroidism, which in turn can cause fetal and neonatal skeletal demineralization, subperiosteal bone resorption, osteitis fibrosa cystica and neonatal seizures.

    8.2 Lactation

    Risk Summary

    Calcium is present in human milk. Administration of the approved recommended dose of calcium chloride injection to the mother is not expected to cause harm to a breastfed infant. There is no information on the effects of calcium chloride injection on the breastfed infant or on milk production. The developmental and health benefits of breastfeeding should be considered along with the mother’s clinical need for calcium chloride injection and any potential adverse effects on the breastfed infant from calcium chloride injection or from the underlying maternal condition.

    8.4 Pediatric Use

    The safety and effectiveness of calcium chloride injection for the treatment of acute symptomatic hypocalcemia have been established in pediatric patients.

    The use of calcium chloride injection is contraindicated in newborns if they require (or are expected to require) ceftriaxone intravenous treatment because of the risk of precipitation of ceftriaxone-calcium, regardless of whether these products would be received at different times or through separate intravenous lines [see Contraindications (4) and Warnings and Precautions (5.1)].

    In pediatric patients older than 28 days of age, calcium chloride injection and ceftriaxone intravenous solutions may be administered sequentially one after another if infusion lines at different sites are used, infusion lines are replaced, or infusion lines are thoroughly flushed between infusions with physiological salt solution to avoid precipitation. Do not mix or administer calcium chloride injection simultaneously with ceftriaxone, even if using different infusion lines or different infusion sites as it can lead to precipitation of ceftriaxone-calcium.

    Calcium chloride injection contains aluminum that may be associated with central nervous system and bone toxicity. Because of immature renal function, preterm infants receiving prolonged parenteral nutrition treatment with calcium chloride injection may be at higher risk of aluminum toxicity [see Warnings and Precautions (5.2)].

    8.5 Geriatric Use

    Clinical studies of calcium chloride injection did not include sufficient numbers of patients 65 years of age and older to determine whether they respond differently from younger adult patients.

    8.6 Renal Impairment

    The use of calcium chloride injection in patients with renal impairment may increase the risk of a higher calcium-phosphorus product. For patients with renal impairment, initiate calcium chloride injection at the lowest recommended dose within the recommended dose range [see Dosage and Administration (2.2)]. Monitor serum calcium levels frequently based on the severity of the renal impairment and the risk of a high calcium-phosphorus product (e.g., every 4 hours).

  • 10 OVERDOSAGE

    Overdosage of calcium chloride injection may lead to hypercalcemia. Symptoms of hypercalcemia typically develop when the total serum calcium concentration is ≥ 12 mg/dL and include shortening of QT interval, bradycardia, hypertension, anorexia, nausea, vomiting, bowel hypomotility and constipation, muscle weakness, bone pain, decreased concentration, depression, weakness, fatigue, confusion, hallucinations, disorientation, hypotonicity, seizures and coma. Hypercalcemia effects on kidney include diminished ability to concentrate urine and diuresis.

    In the event of overdosage, promptly discontinue calcium chloride injection, the patient should be re­-evaluated and appropriate countermeasures should be instituted, if necessary [see Warnings and Precautions (5), Adverse Reactions (6)].

  • 11 DESCRIPTION

    10% Calcium Chloride Injection, USP is a sterile, nonpyrogenic, hypertonic, clear, colorless solution for single administration only. Each mL contains 100 mg (1.4 mEq/mL) of calcium chloride, dihydrate (1.4 mEq each of Ca++ and Cl−) in water for injection. It is provided in a 10 mL single-dose syringe and 10 mL single-dose vial for intravenous injection. The solution contains no bacteriostat, antimicrobial agent or added buffer. The pH of 10% calcium chloride injection, USP is between 5.5 to 7.5 when diluted with water for injection to make a 5% solution. May contain hydrochloric acid and/or sodium hydroxide for pH adjustment. The osmolar concentration is 2.04 mOsmol/mL (calc.). 10% calcium chloride injection, USP is oxygen sensitive.

    Calcium chloride dihydrate, USP is chemically designated CaCl2 2H2O (dihydrate) and its structural formula is as below:

    1

    It appears as white, hard, odorless fragments or granules. It is deliquescent. It is very soluble in boiling water, freely soluble in water, in alcohol and in boiling alcohol.

    Calcium chloride injection, USP contains no more than 1,000 mcg/L of aluminum [see Warnings and Precautions (5.2)].

  • 12 CLINICAL PHARMACOLOGY

    12.1 Mechanism of Action

    Intravenous administration of calcium chloride increases serum ionized calcium concentration. Calcium chloride dissociates into ionized calcium in plasma.

    12.2 Pharmacodynamics

    The exposure-response relationship and time course of pharmacodynamic response for the safety and effectiveness of calcium chloride injection have not been fully characterized.

    12.3 Pharmacokinetics

    Absorption

    Calcium chloride injection is 100% bioavailable following intravenous injection.

    Distribution

    Calcium in the body is distributed mainly in skeleton (99%) and 1% is distributed within the extracellular fluids and soft tissues. About 50% of total serum calcium is in the ionized form and represents the biologically active part; 8% to 10% serum calcium is bound to organic and inorganic acid, respectively; and approximately 40% is protein-bound (primarily to albumin).

    Elimination

    Metabolism

    Calcium itself does not undergo direct metabolism.

    Excretion

    Calcium is excreted by the kidney through a combination of glomerular filtration and tubular reabsorption. A significant increase in urinary excretion of calcium was observed during and after intravenous infusion of calcium chloride.

    Specific Populations

    The effect of age, sex, race, ethnicity, renal or hepatic impairment on the pharmacokinetics of calcium have not been evaluated in clinical studies.

  • 13 NONCLINICAL TOXICOLOGY

    13.1 Carcinogenesis, Mutagenesis, Impairment of Fertility

    Carcinogenicity, mutagenicity and fertility have not been assessed with calcium chloride injection.

  • 16 HOW SUPPLIED/STORAGE AND HANDLING

    10% Calcium Chloride Injection, USP is a clear, colorless solution supplied as follows:

    Unit of Sale and Product Description StrengthNDC

    10 mL Single-Dose Glass Syringe in 1 Carton

    Unit of 24

    1,000 mg/10 mL

    (100 mg/mL)

    NDC: 70121-2308-1

    NDC: 70121-2308-4

    10 mL Single-Dose Vial

    10 x 10 mL Single-Dose Vials in 1 Carton

    1,000 mg/10 mL

    (100 mg/mL)

    NDC: 70121-2309-1

    NDC: 70121-2309-7

    The 100 mg/mL concentration represents 27 mg or 1.4 mEq of elemental calcium per mL of solution.

    Store at 20° to 25°C (68° to 77°F); excursions permitted between 15° to 30°C (59° to 86°F) [see USP Controlled Room Temperature].

  • 17 PATIENT COUNSELING INFORMATION

    Inform patients or caregivers of the following risks of calcium chloride injection:

    Arrhythmias with Concomitant Digoxin Use

    Arrhythmias may occur if calcium chloride injection and Digoxin are administered together [see Warnings and Precautions (5.3)].

    Tissue Necrosis and Calcinosis

    Administration of calcium chloride injection may result in calcinosis cutis including tissue necrosis, ulceration and secondary infection. [see Warnings and Precautions (5.4)].

    Aluminum Toxicity

    Calcium chloride injection contains aluminum that may be toxic [see Warnings and Precautions (5.5)].

    10 mL Single-Dose Pre-Filled Syringe is Manufactured by:

    Amneal Pharmaceuticals Pvt. Ltd.

    Ahmedabad 382213, INDIA

    10 mL Single-Dose Vial is Manufactured by:

    Amneal Pharmaceuticals Pvt. Ltd.

    Ahmedabad 382110, INDIA

    Distributed by:

    Amneal Pharmaceuticals LLC  

    Bridgewater, NJ 08807

    Rev. 07-2024-01

  • PRINCIPAL DISPLAY PANEL

    NDC: 70121-2308-1

    10% Calcium Chloride Injection USP, 1,000 mg/ 10 mL (100 mg/mL)

    10 mL Syringe Label

    Rx only

    Amneal Pharmaceuticals LLC

    2

    NDC: 70121-2308-1

    10% Calcium Chloride Injection USP, 1,000 mg/ 10 mL (100 mg/mL)

    10 mL Syringe Carton Label 

    Rx only

    Amneal Pharmaceuticals LLC

    3

     

    NDC: 70121-2308-4

    10% Calcium Chloride Injection USP, 1,000 mg/ 10 mL (100 mg/mL)

    24 x 10 mL Syringe Carton Label

    Rx only

    Amneal Pharmaceuticals LLC

    4 

    NDC: 70121-2309-1

    10% Calcium Chloride Injection USP, 1,000 mg/ 10 mL (100 mg/mL)

    10 mL Vial Label

    Rx only

    Amneal Pharmaceuticals LLC

    4

    NDC: 70121-2309-7

    10% Calcium Chloride Injection USP, 1,000 mg/ 10 mL (100 mg/mL)

    10 x 10 mL Vial Carton Label

    Rx only

    Amneal Pharmaceuticals LLC

    6
  • INGREDIENTS AND APPEARANCE
    CALCIUM CHLORIDE 
    calcium chloride injection, solution
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC: 70121-2308
    Route of AdministrationINTRAVENOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CALCIUM CHLORIDE (UNII: M4I0D6VV5M) (CALCIUM CATION - UNII:2M83C4R6ZB, CHLORIDE ION - UNII:Q32ZN48698) CALCIUM CHLORIDE100 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC: 70121-2308-424 in 1 CARTON07/17/2024
    1NDC: 70121-2308-11 in 1 CARTON
    110 mL in 1 SYRINGE, GLASS; Type 2: Prefilled Drug Delivery Device/System (syringe, patch, etc.)
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    ANDAANDA21752407/17/2024
    CALCIUM CHLORIDE 
    calcium chloride injection, solution
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC: 70121-2309
    Route of AdministrationINTRAVENOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CALCIUM CHLORIDE (UNII: M4I0D6VV5M) (CALCIUM CATION - UNII:2M83C4R6ZB, CHLORIDE ION - UNII:Q32ZN48698) CALCIUM CHLORIDE100 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC: 70121-2309-710 in 1 CARTON07/17/2024
    1NDC: 70121-2309-110 mL in 1 VIAL, GLASS; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    ANDAANDA21752407/17/2024
    Labeler - Amneal Pharmaceuticals LLC (827748190)
    Establishment
    NameAddressID/FEIBusiness Operations
    Amneal Pharmaceuticals Private Limited860156658analysis(70121-2308) , manufacture(70121-2308) , pack(70121-2308) , sterilize(70121-2308)
    Establishment
    NameAddressID/FEIBusiness Operations
    Amneal Pharmaceuticals Private Limited675474666analysis(70121-2309) , label(70121-2309) , manufacture(70121-2309) , pack(70121-2309) , sterilize(70121-2309)
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