Doxorubicin Injection

  • Generic name

    doxorubicin hydrochloride

  • Brand reference

    Adriamycin PFS®

  • Strength

    10mg / 5ml

  • DIN

    02409275

  • Therapeutic class

    Antineoplastic Agent

  • Therapeutic area

    Oncology


  • Package size

    Vial 25 mL
    Vial 5 mL
    Vial 100 mL

  • Product code

    71843-0025
    71843-0105
    71843-0040

  • UPC

    068510159601
    068510159328
    068510159618

  • Generic name:

    doxorubicin hydrochloride

  • Brand reference:

    Adriamycin PFS®

  • Product code:

    71843-0025
    71843-0105
    71843-0040

  • Strength

    10mg / 5ml

  • DIN

    02409275

  • UPC:

    068510159601
    068510159328
    068510159618

  • Therapeutic class

    Antineoplastic Agent

  • Therapeutic area:

    Oncology

  • Package size:

    Vial 25 mL
    Vial 5 mL
    Vial 100 mL

Composition

Active ingredient

doxorubicin hydrochloride


Non-medicinal ingredients

sodium chloride, hydrochloric acid (for ph adjustment), sodium hydroxide (for ph adjustment) and water for injection

Product characteristics

  • Dosage form

    solution for injection

  • Shape

    -

  • Marking 1

    -

  • Marking 2

    -

  • Colour

    red

  • Secondary colour

    orange

  • Scored

    -

  • Flavour

    -

  • Gluten

    currently not available

  • Latex

    no

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.