Teva-Telmisartan HCTZ

  • Generic name

    telmisartan/hydrochlorothiazide

  • Brand reference

    Micardis Plus®

  • Strength

    80/12.5 mg

  • DIN

    02330288

  • Therapeutic class

    Angiotensin II AT1 Receptor Blocker

  • Therapeutic area

    Cardiovascular

  • Package size

    Bottle 500
    Blister 30
    Bottle 100

  • Product code

    84252-0070
    84252-0127
    84252-0040

  • UPC

    068510181473
    068510181480
    068510181466

  • Generic name:

    telmisartan/hydrochlorothiazide

  • Brand reference:

    Micardis Plus®

  • Product code:

    84252-0070
    84252-0127
    84252-0040

  • Strength

    80/12.5 mg

  • DIN

    02330288

  • UPC:

    068510181473
    068510181480
    068510181466

  • Therapeutic class

    Angiotensin II AT1 Receptor Blocker

  • Therapeutic area:

    Cardiovascular

  • Package size:

    Bottle 500
    Blister 30
    Bottle 100

Composition

Active ingredient

telmisartan/hydrochlorothiazide


Non-medicinal ingredients

hydroxy propyl cellulose, hydroxyl propyl methyl cellulose, lactose monohydrate, meglumine, mannitol, magnesium stearate, purified water, red iron oxide (for 80/12.5 mg only), sodium hydroxide, sorbitol, talc and yellow iron oxide ( for 80/12.5 mg only)

Product characteristics

  • Dosage form

    tablet

  • 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.