Teva-Donepezil

  • Generic name

    donepezil hydrochloride

  • Brand reference

    Aricept®

  • Strength

    10 mg

  • DIN

    02340615

  • Therapeutic class

    Cholinesterase Inhibitor

  • Therapeutic area

    Alzheimer Therapy

  • Package size

    Bottle 100
    Bottle 30

  • Product code

    71756-0040
    71756-0027

  • UPC

    068510149466
    068510149435

  • Generic name:

    donepezil hydrochloride

  • Brand reference:

    Aricept®

  • Product code:

    71756-0040
    71756-0027

  • Strength

    10 mg

  • DIN

    02340615

  • UPC:

    068510149466
    068510149435

  • Therapeutic class

    Cholinesterase Inhibitor

  • Therapeutic area:

    Alzheimer Therapy

  • Package size:

    Bottle 100
    Bottle 30

Composition

Active ingredient

donepezil hydrochloride


Non-medicinal ingredients

hypromellose, lactose monohydrate, magnesium stearate, microcrystalline cellulose, polyethylene glycol, pregelatinised starch, talc and titanium dioxide. the 10 mg tablets also contain iron oxide yellow as a colourant.

Product characteristics

  • Dosage form

    tablet

  • Shape

    round, biconvex

  • Marking 1

    rph D51

  • Marking 2

    D82

  • Colour

    yellow

  • 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.