Active substanceSodium chlorideSodium chloride
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  • Dosage form: & nbspsolvent for the preparation of dosage forms for injection
    Composition:

    Per 1 ml: active substance: sodium chloride - 9 mg; adjuvant: water for injection - up to 1 ml.

    Description:Transparent colorless liquid.
    Pharmacotherapeutic group:Solvent
    ATX: & nbsp

    B.05.C.B.01   Sodium chloride

    B.05.X.A.03   Sodium chloride

    Indications:

    To dissolve and dilute drugs for their further injection.

    Contraindications:

    It can not be used for dissolution and dilution of medicinal products, if another solvent is indicated as an obligatory solvent for them.

    Dosing and Administration:

    The route and mode of administration is determined by the drug to be dissolved or diluted.

    Preparation of solutions of medicinal preparations using sterile sodium chloride is carried out in aseptic conditions (opening of ampoules, filling of syringe and containers with medicinal preparations). The amount of sodium chloride for the preparation of a solution of a specific preparation is determined by the instruction for the medical use of the latter or, depending on the situation, by the doctor.
    Interaction:

    The drug is compatible with colloid hemodynamic blood substitutes. When mixed with other drugs, visual compatibility testing (the nevertheless, invisible and therapeutic incompatibility is possible).

    Special instructions:

    The drug should not be mixed with oily solutions for injection.

    Effect on the ability to drive transp. cf. and fur:The information on this section is set out in the medical instructions for the dissolved or diluted drug.
    Form release / dosage:

    Solvent for preparing dosage forms for injection 0.9%.

    Packaging:

    For 2 ml, 5 ml or 10 ml in the ampoules of neutral glass HC-3. 10 ampoules together with the instruction for use are placed in a pack of cardboard.

    5 ampoules are placed in a contour mesh package made of a polyvinyl chloride film and aluminum foil or without foil.

    2 contour mesh packages along with the instruction for use are placed in a pack of cardboard.

    In each pack insert knife ampoule or scarifier. When packing ampoules with a break point or a fracture ring, the ampoule knife or scarifier is not inserted.
    Storage conditions:

    In the dark place at a temperature of 2 to 30 ° C.

    Keep out of the reach of children.

    Shelf life:

    5 years. Do not use after the expiration date.

    Terms of leave from pharmacies:On prescription
    Registration number:LP-001542
    Date of registration:28.02.2012 / 31.03.2017
    Expiration Date:Unlimited
    The owner of the registration certificate:Armavir Biofactory, FKPArmavir Biofactory, FKP Russia
    Manufacturer: & nbsp
    Information update date: & nbsp15.06.2018
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