Active substanceNifedipineNifedipine
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  • Dosage form: & nbspExtended-release tablets coated with a film sheath
    Composition:1 tablet contains:
    CORE
    Active substance: Nifedipine 20.00 mg
    Excipients: Microcrystalline cellulose is 57.70 mg, glyceryl palmitostearate is 8.10 mg, talc is 1.60 mg, silicon is dioxicolloid, anhydrous is 0.35 mg, sodium lauryl sulfate is 0.80 mg, magnesium stearate 0.45 mg, povidone - 1.00 mg;
    SHELL
    Methacrylic acid copolymer 0.820 mg, talc 1.647 mg, titanium dioxide (E171) 0.693 mg, macrogol 0.167 mg, quinoline yellow color (E104) 0.0057 mg.
    Pharmacotherapeutic group:blocker of "slow" calcium channels
    ATX: & nbsp

    C.08.C.A.05   Nifedipine

    Form release / dosage:Tablets, film-coated, prolonged action, 20 mg. To 15 tablets at blister of combined material PVC / PVDC - aluminum foil. To 2 blisters in a cardboard box together with instructions for use.
    Storage conditions:In dry, the dark place at a temperature of no higher than 25 degrees.
    Shelf life:5 years.
    Terms of leave from pharmacies:On prescription
    Registration number:П N013465 / 01
    Date of registration:19.11.2007
    The owner of the registration certificate:KRKA, dd, Novo mesto, AOKRKA, dd, Novo mesto, AO
    Manufacturer: & nbsp
    Representation: & nbspKRKA, dd, Novo mesto, AOKRKA, dd, Novo mesto, AO
    Information update date: & nbsp19.11.2013
    Illustrated instructions
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