Teva-Quinine

  • Generic name

    quinine sulfate

  • Brand reference

    Quinine®

  • Strength

    200 mg

  • DIN

    00021008

  • Therapeutic class

    Antimalarial Agent

  • Therapeutic area

    Anti-Malaria

  • Package size

    Bottle 100
    Bottle 500

  • Product code

    81752-0040
    81752-0070

  • UPC

    068510499400
    068510499707

  • Generic name:

    quinine sulfate

  • Brand reference:

    Quinine®

  • Product code:

    81752-0040
    81752-0070

  • Strength

    200 mg

  • DIN

    00021008

  • UPC:

    068510499400
    068510499707

  • Therapeutic class

    Antimalarial Agent

  • Therapeutic area:

    Anti-Malaria

  • Package size:

    Bottle 100
    Bottle 500

Composition

Active ingredient

quinine sulfate


Non-medicinal ingredients

ammonium hydroxide, black iron oxide, butyl alcohol, colloidal silicon dioxide, dehydrated alcohol, gelatin, isopropyl alcohol, lactose monohydrate, magnesium stearate, potassium hydroxide, pregelatinized starch, propylene glycol, purified water, shellac, sodium lauryl sulfate and talc.

Product characteristics

  • Dosage form

    capsule

  • Shape

    -

  • Marking 1

    -

  • Marking 2

    -

  • Colour

    -

  • Secondary colour

    -

  • Scored

    -

  • Flavour

    -

  • Gluten

    currently not available

  • Latex

    not applicable

Disclaimers

All information about raw materials and/or allergen information for Teva Canada’s products is obtained from our suppliers and/or third-party affiliates and is based on their records.

Please be advised that the Medical Information department is not always notified of change in third-party affiliates and/or change in suppliers of the active and inactive ingredients that may occur over time, and all information provided herein is based on our last records on file.

Our manufacturing sites are not certified gluten-free. Raw materials and finished products are not tested for the presence of gluten. Therefore, the presence of trace amounts of gluten in the raw materials and in the finished products cannot be excluded.

"Latex" refers to NATURAL RUBBER LATEX. We cannot guarantee that there is no latex in the outer packaging, or that the medication or packaging haven’t come into contact with latex at any point during the manufacturing process; however, this is very unlikely due to the strict GMP procedures that are in place in all of our manufacturing facilities. Employees in the manufacturing and/or packaging facilities may be wearing latex gloves.

Product monograph/consumer information leaflet


View monograph

Notice

We are modifying our product names to align with our corporate name change. Accordingly, please expect product monographs to contain the “Novo-”, “ratio-”, “ACT”, "CO" prefix or the new “Teva” prefix. These prefixes may be used interchangeably on the website.

Should you have any questions about our product names or our corporate name change, please do not hesitate to contact us. Our Customer Care department can be reached at 1-800-268-4127 regarding your inquiry.