ACT Temozolomide

  • Generic name

    temozolomide

  • Brand reference

    Temodal®

  • Strength

    20 mg

  • DIN

    02395274

  • Therapeutic class

    Antineoplastic Agent

  • Therapeutic area

    Oncology

  • Package size

    Bottle 5

  • Product code

    17226-1005

  • UPC

    830790004984

  • Generic name:

    temozolomide

  • Brand reference:

    Temodal®

  • Product code:

    17226-1005

  • Strength

    20 mg

  • DIN

    02395274

  • UPC:

    830790004984

  • Therapeutic class

    Antineoplastic Agent

  • Therapeutic area:

    Oncology

  • Package size:

    Bottle 5

Composition

Active ingredient

temozolomide


Non-medicinal ingredients

colloidal silicon dioxide, lactose anhydrous, sodium starch glycolate, stearic acid and tartaric acid; capsule shells contain gelatin and, titanium dioxide and branded with black printing ink consisting of shellac, dehydrated alcohol, isopropyl alcohol, butyl alcohol, propylene glycol, strong ammonia solution, black iron oxide and potassium hydroxide, yellow iron oxide.

Product characteristics

  • Dosage form

    capsule

  • Shape

    -

  • Marking 1

    TMZ

  • Marking 2

    20

  • Colour

    yellow

  • Secondary colour

    white

  • 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.