ACT Propofol

  • Generic name

    propofol

  • Brand reference

    Diprivan®

  • Strength

    10mg/ml

  • DIN

    02437961

  • Therapeutic class

    Anesthetic/Sedative

  • Therapeutic area

    Anesthetics

  • Package size

    Vial 20x50ml
    Vial 25x20ml
    Vial 10x100ml

  • Product code

    18501-1001
    18500-1001
    18502-1001

  • UPC

    830790006452
    830790006445
    830790006469

  • Generic name:

    propofol

  • Brand reference:

    Diprivan®

  • Product code:

    18501-1001
    18500-1001
    18502-1001

  • Strength

    10mg/ml

  • DIN

    02437961

  • UPC:

    830790006452
    830790006445
    830790006469

  • Therapeutic class

    Anesthetic/Sedative

  • Therapeutic area:

    Anesthetics

  • Package size:

    Vial 20x50ml
    Vial 25x20ml
    Vial 10x100ml

Composition

Active ingredient

propofol


Non-medicinal ingredients

egg phospholipids (12 mg/mL), glycerin (22.5 mg/mL), sodium benzoate (1 mg/mL), soybean oil (100 mg/mL) and water for injection with sodium hydroxide to adjust pH.

Product characteristics

  • Dosage form

    solution

  • Shape

    -

  • Marking 1

    -

  • Marking 2

    -

  • Colour

    white

  • 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.