Label: POTASSIUM CHLORIDE IN DEXTROSE AND SODIUM CHLORIDE- dextrose monohydrate, sodium chloride, and potassium chloride injection, solution

  • NDC Code(s): 0409-7107-09, 0409-7109-09, 0409-7901-03, 0409-7901-09, view more
    0409-7902-03, 0409-7902-09, 0409-7903-09, 0409-7904-09, 0409-7991-09, 0409-7992-09, 0409-7993-09, 0409-7997-09, 0409-7998-03, 0409-7998-09
  • Packager: Hospira, Inc.
  • Category: HUMAN PRESCRIPTION DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: New Drug Application

Drug Label Information

Updated March 2, 2017

If you are a consumer or patient please visit this version.

  • SPL UNCLASSIFIED SECTION

    Rx only

    Potassium Chloride in 5% Dextrose and Sodium Chloride Injection, USP

    Flexible Plastic Container

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  • DESCRIPTION

    Intravenous solutions with potassium chloride (I.V. solutions with KCl) are sterile and nonpyrogenic solutions in water for injection. They are for administration by intravenous infusion only.

    See Tables for summary of content and characteristics of these solutions.

    The solutions contain no bacteriostat, antimicrobial agent or added buffer and each is intended only for use as a single-dose injection. When smaller doses are required the unused portion should be discarded.

    These solutions are parenteral fluid, nutrient and/or electrolyte replenishers.

    Dextrose, USP is chemically designated D-glucose, monohydrate (C6H12O6 • H2O), a hexose sugar freely soluble in water. It has the following structural formula:

    structural formula dextrose

    Potassium Chloride, USP is chemically designated KCl, a white granular powder freely soluble in water.

    Sodium Chloride, USP is chemically designated NaCl, a white crystalline powder freely soluble in water.

    Water for Injection, USP is chemically designated H2O.

    The flexible plastic container is fabricated from a specially formulated polyvinylchloride. Water can permeate from inside the container into the overwrap but not in amounts sufficient to affect the solution significantly. Solutions in contact with the plastic container may leach out certain chemical components from the plastic in very small amounts; however, biological testing was supportive of the safety of the plastic container materials. Exposure to temperatures above 25°C/77°F during transport and storage will lead to minor losses in the moisture content. Higher temperatures lead to greater losses. It is unlikely that these minor losses will lead to clinically significant changes within the expiration period.

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  • CLINICAL PHARMACOLOGY

    When administered intravenously, these solutions provide a source of water and potassium chloride with carbohydrate (dextrose) and sodium chloride. See HOW SUPPLIED section for specific concentrations of these various solutions.

    Solutions containing carbohydrate in the form of dextrose restore blood glucose levels and provide calories. Carbohydrate in the form of dextrose may aid in minimizing liver glycogen depletion and exerts a protein-sparing action. Dextrose injected parenterally undergoes oxidation to carbon dioxide and water.

    Intravenous solutions containing potassium chloride are particularly intended to provide needed potassium cation (K+). Potassium is the chief cation of body cells (160 mEq/liter of intracellular water). It is found in low concentration in plasma and extracellular fluids (3.5 to 5.0 mEq/liter in a healthy adult). Potassium plays an important role in electrolyte balance. Normally about 80 to 90% of the potassium intake is excreted in the urine; the remainder in the stools and to a small extent, in the perspiration. The kidney does not conserve potassium well so that during fasting or in patients on a potassium-free diet, potassium loss from the body continues resulting in potassium depletion. A deficiency of either potassium or chloride will lead to a deficit of the other.

    Sodium chloride in water dissociates to provide sodium (Na+) and chloride (Cl) ions. Sodium (Na+) is the principal cation of the extracellular fluid and plays a large part in the therapy of fluid and electrolyte disturbances. Chloride (Cl) has an integral role in buffering action when oxygen and carbon dioxide exchange occurs in the red blood cells. The distribution and excretion of sodium (Na+) and chloride (Cl) are largely under the control of the kidney which maintains a balance between intake and output.

    Water is an essential constituent of all body tissues and accounts for approximately 70% of total body weight. Average normal adult daily requirement ranges from two to three liters (1.0 to 1.5 liters each for insensible water loss by perspiration and urine production).

    Water balance is maintained by various regulatory mechanisms. Water distribution depends primarily on the concentration of electrolytes in the body compartments and sodium (Na+) plays a major role in maintaining physiologic equilibrium.

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  • INDICATIONS AND USAGE

    These solutions are indicated in patients requiring parenteral administration of potassium chloride with minimal carbohydrate calories and sodium chloride.

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  • CONTRAINDICATIONS

    Solutions containing potassium chloride are contraindicated in diseases where high potassium levels may be encountered.

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  • WARNINGS

    Solutions which contain potassium ions should be used with great care, if at all, in patients with hyperkalemia, severe renal failure and in conditions in which potassium retention is present.

    To avoid potassium intoxication, do not infuse these solutions rapidly. In patients with severe renal insufficiency or adrenal insufficiency, administration of potassium chloride may cause potassium intoxication.

    Solutions containing sodium ions should be used with great care, if at all, in patients with congestive heart failure, severe renal insufficiency and in clinical states in which there exists edema with sodium retention.

    In patients with diminished renal function, administration of solutions containing sodium or potassium ions may result in sodium or potassium retention.

    The intravenous administration of these solutions can cause fluid and/or solute overloading resulting in dilution of serum electrolyte concentrations, overhydration, congested states or pulmonary edema.

    The risk of dilutional states is inversely proportional to the electrolyte concentration of administered parenteral solutions. The risk of solute overload causing congested states with peripheral and pulmonary edema is directly proportional to the electrolyte concentrations of such solutions.

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  • PRECAUTIONS

    Clinical evaluation and periodic laboratory determinations are necessary to monitor changes in fluid balance, electrolyte concentrations and acid-base balance during prolonged parenteral therapy or whenever the condition of the patient warrants such evaluation.

    Solutions containing dextrose should be used with caution in patients with known subclinical or overt diabetes mellitus.

    Caution must be exercised in the administration of parenteral fluids, especially those containing sodium ions, to patients receiving corticosteroids or corticotropin.

    Potassium replacement therapy should be guided primarily by serial electrocardiograms. Plasma potassium levels are not necessarily indicative of tissue potassium levels.

    High plasma concentrations of potassium may cause death through cardiac depression, arrhythmias or arrest.

    Potassium-containing solutions should be used with caution in the presence of cardiac disease, particularly in digitalized patients or in the presence of renal disease.

    Care should be exercised to insure that the needle (or catheter) is well within the lumen of the vein and that extravasation does not occur.

    Do not administer unless solution is clear and container is undamaged. Discard unused portion.

    Carcinogenesis, Mutagenesis, Impairment of Fertility:

    Studies with solutions from flexible plastic containers have not been performed to evaluate carcinogenic potential, mutagenic potential or effects on fertility.

    Pregnancy Category C. Animal reproduction studies have not been conducted with dextrose, potassium chloride or sodium chloride. It is also not known whether dextrose, potassium chloride or sodium chloride can cause fetal harm when administered to a pregnant woman or can affect reproduction capacity. Dextrose, potassium chloride or sodium chloride should be given to a pregnant woman only if clearly needed.

    Nursing Mothers:

    Caution should be exercised when solutions from flexible plastic containers are administered to a nursing mother.

    Pediatric Use:

    The safety and effectiveness in the pediatric population are based on the similarity of the clinical conditions of the pediatric and adult populations. In neonates or very small infants the volume of fluid may affect fluid and electrolyte balance.

    Frequent monitoring of serum glucose concentrations is required when dextrose is prescribed to pediatric patients, particularly neonates and low birth weight infants.

    In very low birth weight infants, excessive or rapid administration of dextrose injection may result in increased serum osmolality and possible intracerebral hemorrhage.

    Geriatric Use:

    An evaluation of current literature revealed no clinical experience identifying differences in response between elderly and younger patients. In general, dose selection for an elderly patient should be cautious, usually starting at the low end of the dosing range, reflecting the greater frequency of decreased hepatic, renal, or cardiac function, and of concomitant disease or other drug therapy. Sodium and potassium ions are known to be substantially excreted by the kidney, and the risk of toxic reactions may be greater in patients with impaired renal function. Because elderly patients are more likely to have decreased renal function, care should be taken in dose selection, and it may be useful to monitor renal function.

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  • ADVERSE REACTIONS

    Reactions which may occur because of the solutions or technique of administration include febrile response, infection at the site of injection, venous thrombosis or phlebitis extending from the site of injection, extravasation and hypervolemia.

    If an adverse reaction does occur, discontinue the infusion, evaluate the patient, institute appropriate therapeutic countermeasures and save the remainder of the fluid for examination if deemed necessary.

    Nausea, vomiting, abdominal pain and diarrhea have been reported with potassium therapy. The signs and symptoms of potassium intoxication include paresthesias of the extremities, flaccid paralysis, listlessness, mental confusion, weakness and heaviness of the legs, hypotension, cardiac arrhythmias, heart block, electrocardiographic abnormalities such as disappearance of P waves, spreading and slurring of the QRS complex with development of a biphasic curve and cardiac arrest.

    Potassium-containing solutions are intrinsically irritating to tissues. Therefore, extreme care should be taken to avoid perivascular infiltration. Local tissue necrosis and subsequent sloughing may result if extravasation occurs. Chemical phlebitis and venospasm have also been reported.

    Should perivascular infiltration occur, I.V. administration at that site should be discontinued at once. Local infiltration of the affected area with procaine hydrochloride, 1%, to which hyaluronidase may be added, will often reduce venospasm and dilute the potassium remaining in the tissues locally. Local application of heat may also be helpful.

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  • OVERDOSAGE

    In the event of potassium overdosage, discontinue the infusion immediately and institute intensive corrective therapy to reduce serum potassium levels. See WARNINGS and PRECAUTIONS.

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  • DOSAGE AND ADMINISTRATION

    These solutions should be administered only by intravenous infusion and as directed by the physician. The dose and rate of injection are dependent upon the age, weight and clinical condition of the patient. If the serum potassium level is greater than 2.5 mEq/liter, potassium should be given at a rate not to exceed 10 mEq/hour in a concentration less than 30 mEq/liter. Somewhat faster rates and greater concentrations (usually up to 40 mEq/liter) of potassium may be indicated in patients with more severe potassium deficiency. The total 24-hour dose should not generally exceed 200 mEq of potassium.

    As reported in the literature, the dosage and constant infusion rate of intravenous dextrose must be selected with caution in pediatric patients, particularly neonates and low birth weight infants, because of the increased risk of hyperglycemia/hypoglycemia.

    Drug Interactions

    Additives may be incompatible. Consult with pharmacist, if available. When introducing additives, use aseptic technique, mix thoroughly and do not store.

    Parenteral drug products should be inspected visually for particulate matter and discoloration prior to administration, whenever solution and container permit. See PRECAUTIONS.

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  • INSTRUCTIONS FOR USE

    To Open

    Tear outer wrap at notch and remove solution container. If supplemental medication is desired, follow directions below before preparing for administration. Some opacity of the plastic due to moisture absorption during the sterilization process may be observed. This is normal and does not affect the solution quality or safety. The opacity will diminish gradually.

    To Add Medication

    1. Prepare additive port.
    2. Using aseptic technique and an additive delivery needle of appropriate length, puncture resealable additive port at target area, inner diaphragm and inject. Withdraw needle after injecting medication.
    3. The additive port may be protected by covering with an additive cap.
    4. Mix container contents thoroughly.

    Preparation for Administration

    (Use aseptic technique)

    1. Close flow control clamp of administration set.
    2. Remove cover from outlet port at bottom of container.
    3. Insert piercing pin of administration set into port with a twisting motion until the set is firmly seated. NOTE: See full directions on administration set carton.
    4. Suspend container from hanger.
    5. Squeeze and release drip chamber to establish proper fluid level in chamber.
    6. Open flow control clamp and clear air from set. Close clamp.
    7. Attach set to venipuncture device. If device is not indwelling, prime and make venipuncture.
    8. Regulate rate of administration with flow control clamp.

    WARNING: Do not use flexible container in series connections.

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  • HOW SUPPLIED

    Intravenous solutions with potassium chloride (I.V. solution with KCl) are supplied in single-dose flexible plastic containers. See Tables:


    TABLE 1













    Potassium Chloride

    in 5% Dextrose and

    0.225% Sodium

    Chloride Inj., USP

    COMPOSITION (g/L)

    Approx. Ionic Concentrations (mEq/L)

    mEq

    Potassium

    Size

    (mL)

    Dextrose,

    Hydrous

    Sodium

    Chloride

    Potassium

    Chloride

    Calculated

    Osmolarity

    (mOsmol/L)

    pH

    Sodium

    (Na+)

    Potassium

    (K+)

    Chloride

    (Cl)

    Approximate

    kcal/L

    NDC NO.














    10 mEq


    1000


    50


    2.25


    0.745


    349

    4.2

    (3.5 to 6.5)


    38.5


    10


    48.5


    170


    0409-7997-09














    10 mEq


    500


    50


    2.25


    1.49


    370

    4.2

    (3.5 to 6.5)


    38.5


    20


    58.5


    170


    0409-7901-03














    20 mEq


    1000


    50


    2.25


    1.49


    370

    4.2

    (3.5 to 6.5)


    38.5


    20


    58.5


    170


    0409-7901-09














     30 mEq


    1000


    50


    2.25


    2.24


    389

    4.2

    (3.5 to 6.5)


    38.5


    30


    68.5


    170


    0409-7991-09














    40 mEq



    1000


    50


    2.25


    2.98


    409

    4.2

    (3.5 to 6.5)


    38.5


    40


    78.5


    170


    0409-7992-09




    TABLE 2













    Potassium Chloride

    in 5% Dextrose and

    0.3% Sodium

    Chloride Inj., USP

    COMPOSITION (g/L)

    Approx. Ionic Concentrations (mEq/L)

    mEq

    Potassium

    Size

    (mL)

    Dextrose,

    Hydrous

    Sodium

    Chloride

    Potassium

    Chloride

    Calculated

    Osmolarity

    (mOsmol/L)

    pH

    Sodium

    (Na+)

    Potassium

    (K+)

    Chloride

    (Cl)

    Approximate

    kcal/L

    NDC NO.














    10 mEq


    500


    50


    3.0


    1.49


    395

    4.2

    (3.5 to 6.5)


    51


    20


    71


    170


    0409-7998-03














    20 mEq



    1000


    50


    3.0


    1.49


    395

    4.2

    (3.5 to 6.5)


    51


    20


    71


    170


    0409-7998-09



    TABLE 3













    Potassium Chloride

    in 5% Dextrose and

    0.45% Sodium

    Chloride Inj., USP

    COMPOSITION (g/L)

    Approx. Ionic Concentrations (mEq/L)

    mEq

    Potassium

    Size

    (mL)

    Dextrose,

    Hydrous

    Sodium

    Chloride

    Potassium

    Chloride

    Calculated

    Osmolarity

    (mOsmol/L)

    pH

    Sodium

    (Na+)

    Potassium

    (K+)

    Chloride

    (Cl)

    Approximate

    kcal/L

    NDC NO.














    10 mEq


    1000


    50


    4.5


    0.745


    426

    4.2

    (3.5 to 6.5)


    77


    10


    87


    170


    0409-7993-09














    10 mEq


    500


    50


    4.5


    1.49


    447

    4.2

    (3.5 to 6.5)


    77


    20


    97


    170


    0409-7902-03














    20 mEq


    1000


    50


    4.5


    1.49


    447

    4.2

    (3.5 to 6.5)


    77


    20


    97


    170


    0409-7902-09














    30 mEq


    1000


    50


    4.5


    2.24


    467

    4.2

    (3.5 to 6.5)


    77


    30


    107


    170


    0409-7903-09














    40 mEq



    1000


    50


    4.5


    2.98


    487

    4.2

    (3.5 to 6.5)


    77


    40


    117


    170


    0409-7904-09




    TABLE 4













    Potassium Chloride

    in 5% Dextrose and

    0.9% Sodium

    Chloride Inj., USP

    COMPOSITION (g/L)

    Approx. Ionic Concentrations (mEq/L)

    mEq

    Potassium

    Size

    (mL)

    Dextrose,

    Hydrous

    Sodium

    Chloride

    Potassium

    Chloride

    Calculated

    Osmolarity

    (mOsmol/L)

    pH

    Sodium

    (Na+)

    Potassium

    (K+)

    Chloride

    (Cl)

    Approximate

    kcal/L

    NDC

    NO.














    20 mEq


    1000


    50


    9


    1.49


    600

    4.2

    (3.5 to 6.5)


    154


    20


    174


    170


    0409-7107-09














    40 mEq



    1000


    50


    9


    2.98


    640

    4.2

    (3.5 to 6.5)


    154


    40


    194


    170


    0409-7109-09



    May contain HCl for pH adjustment.


    Store at 20 to 25°C (68 to 77°F). [See USP Controlled Room Temperature.] 

    Protect from freezing.


    Revised: April, 2009







    Printed in USA                                          EN-2100

    Hospira, Inc., Lake Forest, IL 60045 USA

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  • PRINCIPAL DISPLAY PANEL - 1000 mL Bag Label - IM-0031

    20 mEq POTASSIUM

    1000 mL

    NDC 0409-7107-09

    20
    mEq

    POTASSIUM
    CHLORIDE

    in 5% Dextrose and
    0.9% Sodium Chloride
    Injection, USP

    EACH 100 mL CONTAINS POTASSIUM
    CHLORIDE 149 mg; SODIUM CHLORIDE 900 mg;
    DEXTROSE, HYDROUS 5 g IN WATER FOR
    INJECTION. MAY CONTAIN HCl FOR pH
    ADJUSTMENT. ELECTROLYTES PER 1000 mL
    (NOT INCLUDING IONS FOR pH ADJUSTMENT):
    POTASSIUM 20 mEq; SODIUM 154 mEq;
    CHLORIDE 174 mEq.

    600 mOsmol/LITER (CALC.)
    pH 4.2 (3.5 to 6.5)

    ADDITIVES MAY BE INCOMPATIBLE.
    CONSULT WITH PHARMACIST, IF
    AVAILABLE. WHEN INTRODUCING
    ADDITIVES, USE ASEPTIC TECHNIQUE,
    MIX THOROUGHLY AND DO NOT STORE.

    SINGLE-DOSE CONTAINER. FOR I.V. USE.
    USUAL DOSAGE: SEE INSERT. STERILE,
    NONPYROGENIC. USE ONLY IF SOLUTION IS
    CLEAR AND CONTAINER IS UNDAMAGED.
    MUST NOT BE USED IN SERIES CONNECTIONS.

    Rx only

    3
    v

    CONTAINS DEHP

    ©HOSPIRA 2004
    IM-0031 (4/04)
    PRINTED IN USA

    HOSPIRA, INC., LAKE FOREST, IL 60045 USA

    Hospira

    PRINCIPAL DISPLAY PANEL - 1000 mL Bag Label - IM-0031
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  • PRINCIPAL DISPLAY PANEL - 1000 mL Bag Label - IM-0034

    40 mEq POTASSIUM

    1000 mL

    NDC 0409-7109-09

    40
    mEq

    POTASSIUM
    CHLORIDE

    in 5% Dextrose and
    0.9% Sodium Chloride
    Injection, USP

    EACH 100 mL CONTAINS POTASSIUM
    CHLORIDE 298 mg; SODIUM CHLORIDE 900 mg;
    DEXTROSE, HYDROUS 5 g IN WATER FOR
    INJECTION. MAY CONTAIN HCl FOR pH
    ADJUSTMENT. ELECTROLYTES PER 1000 mL
    (NOT INCLUDING IONS FOR pH ADJUSTMENT):
    POTASSIUM 40 mEq; SODIUM 154 mEq;
    CHLORIDE 194 mEq.

    640 mOsmol/LITER (CALC.)
    pH 4.2 (3.5 to 6.5)

    ADDITIVES MAY BE INCOMPATIBLE.
    CONSULT WITH PHARMACIST, IF
    AVAILABLE. WHEN INTRODUCING
    ADDITIVES, USE ASEPTIC TECHNIQUE,
    MIX THOROUGHLY AND DO NOT STORE.

    SINGLE-DOSE CONTAINER. FOR I.V. USE.
    USUAL DOSAGE: SEE INSERT. STERILE,
    NONPYROGENIC. USE ONLY IF SOLUTION IS
    CLEAR AND CONTAINER IS UNDAMAGED.
    MUST NOT BE USED IN SERIES CONNECTIONS.

    Rx ONLY

    3
    v

    CONTAINS DEHP

    ©HOSPIRA 2004
    IM-0034 (4/04)

    PRINTED IN USA

    HOSPIRA, INC., LAKE FOREST, IL 60045 USA

    Hospira

    PRINCIPAL DISPLAY PANEL - 1000 mL Bag Label - IM-0034
    Close
  • PRINCIPAL DISPLAY PANEL - 1000 mL Bag Label - IM-0086

    30 mEq POTASSIUM

    1000 mL

    NDC 0409-7903-09

    30
    mEq

    POTASSIUM
    CHLORIDE

    in 5% Dextrose and
    0.45% Sodium Chloride
    Injection, USP

    EACH 100 mL CONTAINS POTASSIUM
    CHLORIDE 224 mg; SODIUM CHLORIDE 450 mg;
    DEXTROSE, HYDROUS 5 g IN WATER FOR
    INJECTION. MAY CONTAIN HCl FOR pH
    ADJUSTMENT. ELECTROLYTES PER 1000 mL
    (NOT INCLUDING IONS FOR pH ADJUSTMENT):
    POTASSIUM 30 mEq; SODIUM 77 mEq;
    CHLORIDE 107 mEq.

    467 mOsmol/LITER (CALC.)
    pH 4.2 (3.5 to 6.5)

    ADDITIVES MAY BE INCOMPATIBLE.
    CONSULT WITH PHARMACIST, IF
    AVAILABLE. WHEN INTRODUCING
    ADDITIVES, USE ASEPTIC TECHNIQUE,
    MIX THOROUGHLY AND DO NOT STORE.

    SINGLE-DOSE CONTAINER. FOR I.V. USE.
    USUAL DOSAGE: SEE INSERT. STERILE,
    NONPYROGENIC. USE ONLY IF SOLUTION IS
    CLEAR AND CONTAINER IS UNDAMAGED.
    MUST NOT BE USED IN SERIES CONNECTIONS.

    Rx ONLY

    3
    v

    CONTAINS DEHP

    ©HOSPIRA 2004
    IM-0086 (4/04)
    PRINTED IN USA

    HOSPIRA, INC., LAKE FOREST, IL 60045 USA

    Hospira

    PRINCIPAL DISPLAY PANEL - 1000 mL Bag Label - IM-0086
    Close
  • PRINCIPAL DISPLAY PANEL - 1000 mL Bag Label - IM-0087

    40 mEq POTASSIUM

    1000 mL

    NDC 0409-7904-09

    40
    mEq

    POTASSIUM
    CHLORIDE

    in 5% Dextrose and
    0.45% Sodium Chloride
    Injection, USP

    EACH 100 mL CONTAINS POTASSIUM
    CHLORIDE 298 mg; SODIUM CHLORIDE 450 mg;
    DEXTROSE, HYDROUS 5 g IN WATER FOR
    INJECTION. MAY CONTAIN HCl FOR pH
    ADJUSTMENT. ELECTROLYTES PER 1000 mL
    (NOT INCLUDING IONS FOR pH ADJUSTMENT):
    POTASSIUM 40 mEq; SODIUM 77 mEq;
    CHLORIDE 117 mEq.

    487 mOsmol/LITER (CALC.)
    pH 4.2 (3.5 to 6.5)

    ADDITIVES MAY BE INCOMPATIBLE.
    CONSULT WITH PHARMACIST, IF
    AVAILABLE. WHEN INTRODUCING
    ADDITIVES, USE ASEPTIC TECHNIQUE,
    MIX THOROUGHLY AND DO NOT STORE.

    SINGLE-DOSE CONTAINER. FOR I.V. USE.
    USUAL DOSAGE: SEE INSERT. STERILE,
    NONPYROGENIC. USE ONLY IF SOLUTION IS
    CLEAR AND CONTAINER IS UNDAMAGED.
    MUST NOT BE USED IN SERIES CONNECTIONS.

    Rx ONLY

    3
    v

    CONTAINS DEHP

    ©HOSPIRA 2004
    IM-0087 (4/04)
    PRINTED IN USA

    HOSPIRA, INC., LAKE FOREST, IL 60045 USA

    Hospira

    PRINCIPAL DISPLAY PANEL - 1000 mL Bag Label - IM-0087
    Close
  • PRINCIPAL DISPLAY PANEL - 1000 mL Bag Label - IM-0088

    30 mEq POTASSIUM

    1000 mL

    NDC 0409-7991-09

    30
    mEq

    POTASSIUM
    CHLORIDE

    in 5% Dextrose and
    0.225% Sodium Chloride
    Injection, USP

    EACH 100 mL CONTAINS POTASSIUM CHLORIDE
    224 mg; SODIUM CHLORIDE 225 mg; DEXTROSE,
    HYDROUS 5 g IN WATER FOR INJECTION. MAY
    CONTAIN HCl FOR pH ADJUSTMENT.

    ELECTROLYTES PER 1000 mL (NOT INCLUDING
    IONS FOR pH ADJUSTMENT): POTASSIUM
    30 mEq; SODIUM 38.5 mEq; CHLORIDE 68.5 mEq.

    389 mOsmol/LITER (CALC.)
    pH 4.2 (3.5 to 6.5)

    ADDITIVES MAY BE INCOMPATIBLE.
    CONSULT WITH PHARMACIST, IF AVAILABLE.
    WHEN INTRODUCING ADDITIVES,
    USE ASEPTIC TECHNIQUE, MIX THOROUGHLY
    AND DO NOT STORE.

    SINGLE-DOSE CONTAINER. FOR I.V. USE.
    USUAL DOSAGE: SEE INSERT. STERILE,
    NONPYROGENIC. USE ONLY IF SOLUTION IS CLEAR
    AND CONTAINER IS UNDAMAGED. MUST NOT BE
    USED IN SERIES CONNECTIONS.

    Rx ONLY

    3
    v

    CONTAINS DEHP

    ©HOSPIRA 2004
    IM-0088 (4/04)

    PRINTED IN USA

    HOSPIRA, INC., LAKE FOREST, IL 60045 USA

    Hospira

    PRINCIPAL DISPLAY PANEL - 1000 mL Bag Label - IM-0088
    Close
  • PRINCIPAL DISPLAY PANEL - 1000 mL Bag Label - IM-0089

    40 mEq POTASSIUM

    1000 mL

    NDC 0409-7992-09

    40
    mEq

    POTASSIUM
    CHLORIDE

    in 5% Dextrose and
    0.225% Sodium Chloride
    Injection, USP

    EACH 100 mL CONTAINS POTASSIUM CHLORIDE
    298 mg; SODIUM CHLORIDE 225 mg; DEXTROSE,
    HYDROUS 5 g IN WATER FOR INJECTION. MAY
    CONTAIN HCl FOR pH ADJUSTMENT.

    ELECTROLYTES PER 1000 mL (NOT INCLUDING
    IONS FOR pH ADJUSTMENT): POTASSIUM
    40 mEq; SODIUM 38.5 mEq; CHLORIDE 78.5 mEq.

    409 mOsmol/LITER (CALC.)
    pH 4.2 (3.5 to 6.5)

    ADDITIVES MAY BE INCOMPATIBLE.
    CONSULT WITH PHARMACIST, IF AVAILABLE.
    WHEN INTRODUCING ADDITIVES,
    USE ASEPTIC TECHNIQUE, MIX THOROUGHLY
    AND DO NOT STORE.

    SINGLE-DOSE CONTAINER. FOR I.V. USE.
    USUAL DOSAGE: SEE INSERT. STERILE,
    NONPYROGENIC. USE ONLY IF SOLUTION IS CLEAR
    AND CONTAINER IS UNDAMAGED. MUST NOT BE
    USED IN SERIES CONNECTIONS.

    Rx ONLY

    3
    v

    CONTAINS DEHP

    ©HOSPIRA 2004
    IM-0089 (4/04)

    PRINTED IN USA

    HOSPIRA, INC., LAKE FOREST, IL 60045 USA

    Hospira

    PRINCIPAL DISPLAY PANEL - 1000 mL Bag Label - IM-0089
    Close
  • PRINCIPAL DISPLAY PANEL - 1000 mL Bag Label - IM-0090

    10 mEq POTASSIUM

    1000 mL

    NDC 0409-7993-09

    10
    mEq

    POTASSIUM
    CHLORIDE

    in 5% Dextrose and
    0.45% Sodium Chloride
    Injection, USP

    EACH 100 mL CONTAINS POTASSIUM
    CHLORIDE 74.5 mg; SODIUM CHLORIDE 450 mg;
    DEXTROSE, HYDROUS 5 g IN WATER FOR
    INJECTION. MAY CONTAIN HCl FOR pH
    ADJUSTMENT.

    ELECTROLYTES PER 1000 mL (NOT INCLUDING
    IONS FOR pH ADJUSTMENT): POTASSIUM
    10 mEq; SODIUM 77 mEq; CHLORIDE 87 mEq.

    426 mOsmol/LITER (CALC.)
    pH 4.2 (3.5 to 6.5)

    ADDITIVES MAY BE INCOMPATIBLE.
    CONSULT WITH PHARMACIST, IF AVAILABLE.
    WHEN INTRODUCING ADDITIVES,
    USE ASEPTIC TECHNIQUE, MIX THOROUGHLY
    AND DO NOT STORE.

    SINGLE-DOSE CONTAINER. FOR I.V. USE.
    USUAL DOSAGE: SEE INSERT. STERILE,
    NONPYROGENIC. USE ONLY IF SOLUTION IS
    CLEAR AND CONTAINER IS UNDAMAGED.
    MUST NOT BE USED IN SERIES CONNECTIONS.

    Rx ONLY

    3
    v

    CONTAINS
    DEHP

    PRINTED IN USA

    ©HOSPIRA 2004
    IM-0090 (4/04)

    HOSPIRA, INC., LAKE FOREST, IL 60045 USA

    Hospira

    PRINCIPAL DISPLAY PANEL - 1000 mL Bag Label - IM-0090
    Close
  • PRINCIPAL DISPLAY PANEL - 500 mL Bag Label - IM-0057

    10 mEq POTASSIUM

    500 mL

    NDC 0409-7901-03

    10
    mEq

    POTASSIUM
    CHLORIDE
    in 5% Dextrose and
    0.225% Sodium Chloride Inj., USP

    EACH 100 mL CONTAINS POTASSIUM CHLORIDE 149 mg; SODIUM
    CHLORIDE 225 mg; DEXTROSE, HYDROUS 5 g IN WATER FOR INJECTION.
    MAY CONTAIN HCl FOR pH ADJUSTMENT. ELECTROLYTES PER 1000 mL
    (NOT INCLUDING IONS FOR pH ADJUSTMENT): POTASSIUM 20 mEq;
    SODIUM 38.5 mEq; CHLORIDE 58.5 mEq. 370 mOsmol/LITER (CALC.)
    pH 4.2 (3.5 to 6.5)

    ADDITIVES MAY BE INCOMPATIBLE. CONSULT WITH
    PHARMACIST, IF AVAILABLE. WHEN INTRODUCING
    ADDITIVES, USE ASEPTIC TECHNIQUE, MIX
    THOROUGHLY AND DO NOT STORE.

    SINGLE-DOSE CONTAINER. FOR I.V. USE. USUAL DOSAGE: SEE INSERT.
    STERILE, NONPYROGENIC. USE ONLY IF SOLUTION IS CLEAR AND
    CONTAINER IS UNDAMAGED. MUST NOT BE USED IN SERIES
    CONNECTIONS.

    ©HOSPIRA 2004
    IM-0057 (4/04)
    PRINTED IN USA
    HOSPIRA, INC., LAKE FOREST, IL 60045 USA

    3
    v

    CONTAINS DEHP

    Rx ONLY

    Hospira

    PRINCIPAL DISPLAY PANEL - 500 mL Bag Label - IM-0057
    Close
  • PRINCIPAL DISPLAY PANEL - 500 mL Bag Label - IM-0096

    10 mEq POTASSIUM

    500 mL

    NDC 0409-7998-03

    10
    mEq

    POTASSIUM
    CHLORIDE
    in 5% Dextrose and
    0.3% Sodium Chloride Inj., USP

    EACH 100 mL CONTAINS POTASSIUM CHLORIDE 149 mg; SODIUM
    CHLORIDE 300 mg; DEXTROSE, HYDROUS 5 g IN WATER FOR
    INJECTION. MAY CONTAIN HCl FOR pH ADJUSTMENT.
    ELECTROLYTES PER 1000 mL (NOT INCLUDING IONS FOR pH
    ADJUSTMENT): POTASSIUM 20 mEq; SODIUM 51 mEq; CHLORIDE 71
    mEq. 395 mOsmol/LITER (CALC.)
    pH 4.2 (3.5 to 6.5)

    ADDITIVES MAY BE INCOMPATIBLE.
    CONSULT WITH PHARMACIST, IF AVAILABLE.
    WHEN INTRODUCING ADDITIVES, USE ASEPTIC TECHNIQUE, MIX
    THOROUGHLY AND DO NOT STORE.

    SINGLE-DOSE CONTAINER. FOR I.V. USE. USUAL DOSAGE: SEE
    INSERT. STERILE, NONPYROGENIC. USE
    ONLY IF SOLUTION IS CLEAR AND
    CONTAINER IS UNDAMAGED. MUST NOT
    BE USED IN SERIES CONNECTIONS.

    3
    v

    CONTAINS DEHP

    PRINTED IN USA
    Rx ONLY

    ©HOSPIRA 2004
    IM-0096 (4/04)

    HOSPIRA, INC., LAKE FOREST, IL 60045 USA

    Hospira

    PRINCIPAL DISPLAY PANEL - 500 mL Bag Label - IM-0096
    Close
  • PRINCIPAL DISPLAY PANEL - 500 mL Bag Label - IM-0065

    10 mEq POTASSIUM

    500 mL

    NDC 0409-7902-03

    10
    mEq

    POTASSIUM
    CHLORIDE
    in 5% Dextrose and
    0.45% Sodium Chloride Inj., USP

    EACH 100 mL CONTAINS POTASSIUM CHLORIDE 149 mg; SODIUM
    CHLORIDE 450 mg; DEXTROSE, HYDROUS 5 g IN WATER
    FOR INJECTION. MAY CONTAIN HCl FOR pH ADJUSTMENT.
    ELECTROLYTES PER 1000 mL (NOT INCLUDING IONS FOR pH
    ADJUSTMENT): POTASSIUM 20 mEq; SODIUM 77 mEq; CHLORIDE 97 mEq.

    447 mOsmol/LITER (CALC.)
    pH 4.2 (3.5 to 6.5)

    ADDITIVES MAY BE INCOMPATIBLE. CONSULT WITH
    PHARMACIST, IF AVAILABLE. WHEN INTRODUCING
    ADDITIVES, USE ASEPTIC TECHNIQUE, MIX
    THOROUGHLY AND DO NOT STORE.

    SINGLE-DOSE CONTAINER. FOR I.V. USE. USUAL DOSAGE: SEE INSERT.
    STERILE, NONPYROGENIC. USE ONLY IF SOLUTION IS CLEAR AND
    CONTAINER IS UNDAMAGED. MUST NOT BE USED IN SERIES
    CONNECTIONS.

    Rx ONLY

    3
    v

    CONTAINS DEHP

    PRINTED IN USA
    ©HOSPIRA 2004
    IM-0065 (4/04)
    HOSPIRA, INC., LAKE FOREST, IL 60045 USA

    Hospira

    PRINCIPAL DISPLAY PANEL - 500 mL Bag Label - IM-0065
    Close
  • PRINCIPAL DISPLAY PANEL - 1000 mL Bag Label - IM-0091

    10 mEq POTASSIUM

    1000 mL

    NDC 0409-7997-09

    10
    mEq

    POTASSIUM
    CHLORIDE

    in 5% Dextrose and
    0.225% Sodium Chloride
    Injection, USP

    EACH 100 mL CONTAINS POTASSIUM
    CHLORIDE 74.5 mg; SODIUM CHLORIDE 225 mg;
    DEXTROSE, HYDROUS 5 g IN WATER FOR
    INJECTION. MAY CONTAIN HCl FOR pH
    ADJUSTMENT.

    ELECTROLYTES PER 1000 mL (NOT INCLUDING
    IONS FOR pH ADJUSTMENT): POTASSIUM
    10 mEq; SODIUM 38.5 mEq; CHLORIDE 48.5 mEq.

    349 mOsmol/LITER (CALC.)
    pH 4.2 (3.5 to 6.5)

    ADDITIVES MAY BE INCOMPATIBLE.
    CONSULT WITH PHARMACIST, IF AVAILABLE.
    WHEN INTRODUCING ADDITIVES,
    USE ASEPTIC TECHNIQUE, MIX THOROUGHLY
    AND DO NOT STORE.

    SINGLE-DOSE CONTAINER. FOR I.V. USE.
    USUAL DOSAGE: SEE INSERT. STERILE,
    NONPYROGENIC. USE ONLY IF SOLUTION IS
    CLEAR AND CONTAINER IS UNDAMAGED.
    MUST NOT BE USED IN SERIES CONNECTIONS.

    Rx ONLY

    3
    v

    CONTAINS DEHP

    PRINTED IN USA

    ©HOSPIRA 2004
    IM-0091 (4/04)

    HOSPIRA, INC., LAKE FOREST, IL 60045 USA

    Hospira

    PRINCIPAL DISPLAY PANEL - 1000 mL Bag Label - IM-0091
    Close
  • PRINCIPAL DISPLAY PANEL - Overwrap

    TO OPEN TEAR AT NOTCH

    2
    HDPE

    DO NOT REMOVE FROM OVERWRAP UNTIL READY FOR USE. AFTER REMOVING
    THE OVERWRAP, CHECK FOR MINUTE LEAKS BY SQUEEZING CONTAINER FIRMLY.
    IF LEAKS ARE FOUND, DISCARD SOLUTION AS STERILITY MAY BE IMPAIRED.
    RECOMMENDED STORAGE: ROOM TEMPERATURE (25°C). AVOID EXCESSIVE
    HEAT. PROTECT FROM FREEZING. SEE INSERT.
    98-4321-R14-3/98

    PRINCIPAL DISPLAY PANEL - Overwrap
    Close
  • INGREDIENTS AND APPEARANCE
    POTASSIUM CHLORIDE IN DEXTROSE AND SODIUM CHLORIDE 
    dextrose monohydrate, sodium chloride, and potassium chloride injection, solution
    Product Information
    Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:0409-7107
    Route of Administration INTRAVENOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    DEXTROSE MONOHYDRATE (UNII: LX22YL083G) (ANHYDROUS DEXTROSE - UNII:5SL0G7R0OK) DEXTROSE MONOHYDRATE 50 g  in 1000 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) (SODIUM CATION - UNII:LYR4M0NH37, CHLORIDE ION - UNII:Q32ZN48698) SODIUM CHLORIDE 9 g  in 1000 mL
    POTASSIUM CHLORIDE (UNII: 660YQ98I10) (POTASSIUM CATION - UNII:295O53K152, CHLORIDE ION - UNII:Q32ZN48698) POTASSIUM CHLORIDE 1.49 g  in 1000 mL
    Inactive Ingredients
    Ingredient Name Strength
    WATER (UNII: 059QF0KO0R)  
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0409-7107-09 12 in 1 CASE 12/31/2004
    1 1 in 1 POUCH
    1 1000 mL in 1 BAG; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    NDA NDA019691 12/31/2004
    POTASSIUM CHLORIDE IN DEXTROSE AND SODIUM CHLORIDE 
    dextrose monohydrate, sodium chloride, and potassium chloride injection, solution
    Product Information
    Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:0409-7109
    Route of Administration INTRAVENOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    DEXTROSE MONOHYDRATE (UNII: LX22YL083G) (ANHYDROUS DEXTROSE - UNII:5SL0G7R0OK) DEXTROSE MONOHYDRATE 50 g  in 1000 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) (SODIUM CATION - UNII:LYR4M0NH37, CHLORIDE ION - UNII:Q32ZN48698) SODIUM CHLORIDE 9 g  in 1000 mL
    POTASSIUM CHLORIDE (UNII: 660YQ98I10) (POTASSIUM CATION - UNII:295O53K152, CHLORIDE ION - UNII:Q32ZN48698) POTASSIUM CHLORIDE 2.98 g  in 1000 mL
    Inactive Ingredients
    Ingredient Name Strength
    WATER (UNII: 059QF0KO0R)  
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0409-7109-09 12 in 1 CASE 03/31/2005
    1 1 in 1 POUCH
    1 1000 mL in 1 BAG; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    NDA NDA019691 03/31/2005
    POTASSIUM CHLORIDE IN DEXTROSE AND SODIUM CHLORIDE 
    dextrose monohydrate, sodium chloride, and potassium chloride injection, solution
    Product Information
    Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:0409-7903
    Route of Administration INTRAVENOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    DEXTROSE MONOHYDRATE (UNII: LX22YL083G) (ANHYDROUS DEXTROSE - UNII:5SL0G7R0OK) DEXTROSE MONOHYDRATE 50 g  in 1000 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) (SODIUM CATION - UNII:LYR4M0NH37, CHLORIDE ION - UNII:Q32ZN48698) SODIUM CHLORIDE 4.5 g  in 1000 mL
    POTASSIUM CHLORIDE (UNII: 660YQ98I10) (POTASSIUM CATION - UNII:295O53K152, CHLORIDE ION - UNII:Q32ZN48698) POTASSIUM CHLORIDE 2.24 g  in 1000 mL
    Inactive Ingredients
    Ingredient Name Strength
    WATER (UNII: 059QF0KO0R)  
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0409-7903-09 12 in 1 CASE 11/01/2005
    1 1 in 1 POUCH
    1 1000 mL in 1 BAG; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    NDA NDA018362 11/01/2005
    POTASSIUM CHLORIDE IN DEXTROSE AND SODIUM CHLORIDE 
    dextrose monohydrate, sodium chloride, and potassium chloride injection, solution
    Product Information
    Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:0409-7904
    Route of Administration INTRAVENOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    DEXTROSE MONOHYDRATE (UNII: LX22YL083G) (ANHYDROUS DEXTROSE - UNII:5SL0G7R0OK) DEXTROSE MONOHYDRATE 50 g  in 1000 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) (SODIUM CATION - UNII:LYR4M0NH37, CHLORIDE ION - UNII:Q32ZN48698) SODIUM CHLORIDE 4.5 g  in 1000 mL
    POTASSIUM CHLORIDE (UNII: 660YQ98I10) (POTASSIUM CATION - UNII:295O53K152, CHLORIDE ION - UNII:Q32ZN48698) POTASSIUM CHLORIDE 2.98 g  in 1000 mL
    Inactive Ingredients
    Ingredient Name Strength
    WATER (UNII: 059QF0KO0R)  
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0409-7904-09 12 in 1 CASE 06/03/2005
    1 1 in 1 POUCH
    1 1000 mL in 1 BAG; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    NDA NDA018362 06/03/2005
    POTASSIUM CHLORIDE IN DEXTROSE AND SODIUM CHLORIDE 
    dextrose monohydrate, sodium chloride, and potassium chloride injection, solution
    Product Information
    Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:0409-7991
    Route of Administration INTRAVENOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    DEXTROSE MONOHYDRATE (UNII: LX22YL083G) (ANHYDROUS DEXTROSE - UNII:5SL0G7R0OK) DEXTROSE MONOHYDRATE 50 g  in 1000 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) (SODIUM CATION - UNII:LYR4M0NH37, CHLORIDE ION - UNII:Q32ZN48698) SODIUM CHLORIDE 2.25 g  in 1000 mL
    POTASSIUM CHLORIDE (UNII: 660YQ98I10) (POTASSIUM CATION - UNII:295O53K152, CHLORIDE ION - UNII:Q32ZN48698) POTASSIUM CHLORIDE 2.24 g  in 1000 mL
    Inactive Ingredients
    Ingredient Name Strength
    WATER (UNII: 059QF0KO0R)  
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0409-7991-09 12 in 1 CASE 09/29/2005
    1 1 in 1 POUCH
    1 1000 mL in 1 BAG; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    NDA NDA018365 09/29/2005
    POTASSIUM CHLORIDE IN DEXTROSE AND SODIUM CHLORIDE 
    dextrose monohydrate, sodium chloride, and potassium chloride injection, solution
    Product Information
    Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:0409-7992
    Route of Administration INTRAVENOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    DEXTROSE MONOHYDRATE (UNII: LX22YL083G) (ANHYDROUS DEXTROSE - UNII:5SL0G7R0OK) DEXTROSE MONOHYDRATE 50 g  in 1000 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) (SODIUM CATION - UNII:LYR4M0NH37, CHLORIDE ION - UNII:Q32ZN48698) SODIUM CHLORIDE 2.25 g  in 1000 mL
    POTASSIUM CHLORIDE (UNII: 660YQ98I10) (POTASSIUM CATION - UNII:295O53K152, CHLORIDE ION - UNII:Q32ZN48698) POTASSIUM CHLORIDE 2.98 g  in 1000 mL
    Inactive Ingredients
    Ingredient Name Strength
    WATER (UNII: 059QF0KO0R)  
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0409-7992-09 12 in 1 CASE 09/29/2005
    1 1 in 1 POUCH
    1 1000 mL in 1 BAG; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    NDA NDA018365 09/29/2005
    POTASSIUM CHLORIDE IN DEXTROSE AND SODIUM CHLORIDE 
    dextrose monohydrate, sodium chloride, and potassium chloride injection, solution
    Product Information
    Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:0409-7993
    Route of Administration INTRAVENOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    DEXTROSE MONOHYDRATE (UNII: LX22YL083G) (ANHYDROUS DEXTROSE - UNII:5SL0G7R0OK) DEXTROSE MONOHYDRATE 50 g  in 1000 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) (SODIUM CATION - UNII:LYR4M0NH37, CHLORIDE ION - UNII:Q32ZN48698) SODIUM CHLORIDE 4.5 g  in 1000 mL
    POTASSIUM CHLORIDE (UNII: 660YQ98I10) (POTASSIUM CATION - UNII:295O53K152, CHLORIDE ION - UNII:Q32ZN48698) POTASSIUM CHLORIDE 0.745 g  in 1000 mL
    Inactive Ingredients
    Ingredient Name Strength
    WATER (UNII: 059QF0KO0R)  
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0409-7993-09 12 in 1 CASE 02/28/2005
    1 1 in 1 POUCH
    1 1000 mL in 1 BAG; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    NDA NDA018362 02/28/2005
    POTASSIUM CHLORIDE IN DEXTROSE AND SODIUM CHLORIDE 
    dextrose monohydrate, sodium chloride, and potassium chloride injection, solution
    Product Information
    Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:0409-7901
    Route of Administration INTRAVENOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    DEXTROSE MONOHYDRATE (UNII: LX22YL083G) (ANHYDROUS DEXTROSE - UNII:5SL0G7R0OK) DEXTROSE MONOHYDRATE 50 g  in 1000 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) (SODIUM CATION - UNII:LYR4M0NH37, CHLORIDE ION - UNII:Q32ZN48698) SODIUM CHLORIDE 2.25 g  in 1000 mL
    POTASSIUM CHLORIDE (UNII: 660YQ98I10) (POTASSIUM CATION - UNII:295O53K152, CHLORIDE ION - UNII:Q32ZN48698) POTASSIUM CHLORIDE 1.49 g  in 1000 mL
    Inactive Ingredients
    Ingredient Name Strength
    WATER (UNII: 059QF0KO0R)  
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0409-7901-03 24 in 1 CASE 03/30/2005
    1 1 in 1 POUCH
    1 500 mL in 1 BAG; Type 0: Not a Combination Product
    2 NDC:0409-7901-09 12 in 1 CASE 03/30/2005
    2 1 in 1 POUCH
    2 1000 mL in 1 BAG; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    NDA NDA018365 03/30/2005
    POTASSIUM CHLORIDE IN DEXTROSE AND SODIUM CHLORIDE 
    dextrose monohydrate, sodium chloride, and potassium chloride injection, solution
    Product Information
    Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:0409-7998
    Route of Administration INTRAVENOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    DEXTROSE MONOHYDRATE (UNII: LX22YL083G) (ANHYDROUS DEXTROSE - UNII:5SL0G7R0OK) DEXTROSE MONOHYDRATE 50 g  in 1000 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) (SODIUM CATION - UNII:LYR4M0NH37, CHLORIDE ION - UNII:Q32ZN48698) SODIUM CHLORIDE 3 g  in 1000 mL
    POTASSIUM CHLORIDE (UNII: 660YQ98I10) (POTASSIUM CATION - UNII:295O53K152, CHLORIDE ION - UNII:Q32ZN48698) POTASSIUM CHLORIDE 1.49 g  in 1000 mL
    Inactive Ingredients
    Ingredient Name Strength
    WATER (UNII: 059QF0KO0R)  
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0409-7998-03 24 in 1 CASE 03/31/2005
    1 1 in 1 POUCH
    1 500 mL in 1 BAG; Type 0: Not a Combination Product
    2 NDC:0409-7998-09 12 in 1 CASE 02/28/2005
    2 1 in 1 POUCH
    2 1000 mL in 1 BAG; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    NDA NDA018876 02/28/2005
    POTASSIUM CHLORIDE IN DEXTROSE AND SODIUM CHLORIDE 
    dextrose monohydrate, sodium chloride, and potassium chloride injection, solution
    Product Information
    Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:0409-7902
    Route of Administration INTRAVENOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    DEXTROSE MONOHYDRATE (UNII: LX22YL083G) (ANHYDROUS DEXTROSE - UNII:5SL0G7R0OK) DEXTROSE MONOHYDRATE 50 g  in 1000 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) (SODIUM CATION - UNII:LYR4M0NH37, CHLORIDE ION - UNII:Q32ZN48698) SODIUM CHLORIDE 4.5 g  in 1000 mL
    POTASSIUM CHLORIDE (UNII: 660YQ98I10) (POTASSIUM CATION - UNII:295O53K152, CHLORIDE ION - UNII:Q32ZN48698) POTASSIUM CHLORIDE 1.49 g  in 1000 mL
    Inactive Ingredients
    Ingredient Name Strength
    WATER (UNII: 059QF0KO0R)  
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0409-7902-03 24 in 1 CASE 02/28/2005
    1 1 in 1 POUCH
    1 500 mL in 1 BAG; Type 0: Not a Combination Product
    2 NDC:0409-7902-09 12 in 1 CASE 01/31/2005
    2 1 in 1 POUCH
    2 1000 mL in 1 BAG; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    NDA NDA018362 01/31/2005
    POTASSIUM CHLORIDE IN DEXTROSE AND SODIUM CHLORIDE 
    dextrose monohydrate, sodium chloride, and potassium chloride injection, solution
    Product Information
    Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:0409-7997
    Route of Administration INTRAVENOUS
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    DEXTROSE MONOHYDRATE (UNII: LX22YL083G) (ANHYDROUS DEXTROSE - UNII:5SL0G7R0OK) DEXTROSE MONOHYDRATE 50 g  in 1000 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) (SODIUM CATION - UNII:LYR4M0NH37, CHLORIDE ION - UNII:Q32ZN48698) SODIUM CHLORIDE 2.25 g  in 1000 mL
    POTASSIUM CHLORIDE (UNII: 660YQ98I10) (POTASSIUM CATION - UNII:295O53K152, CHLORIDE ION - UNII:Q32ZN48698) POTASSIUM CHLORIDE 0.745 g  in 1000 mL
    Inactive Ingredients
    Ingredient Name Strength
    WATER (UNII: 059QF0KO0R)  
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0409-7997-09 12 in 1 CASE 01/31/2005 05/01/2010
    1 1 in 1 POUCH
    1 1000 mL in 1 BAG; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    NDA NDA018365 01/31/2005 05/01/2010
    Labeler - Hospira, Inc. (141588017)
    Establishment
    Name Address ID/FEI Business Operations
    Hospira, Inc. 827731089 ANALYSIS(0409-7107, 0409-7109, 0409-7901, 0409-7902, 0409-7903, 0409-7904, 0409-7991, 0409-7992, 0409-7993, 0409-7997, 0409-7998)
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