ACT Buprenorphine/Naloxone

  • Generic name

    buprenorphine hydrochloride and naloxone hydrochloride dihydrate

  • Brand reference

    Suboxone®

  • Strength

    2mg/0.5mg

  • DIN

    02453908

  • Therapeutic class

    Partial Opioid Agonist/Opioid Antagonist

  • Therapeutic area

    Opiate Antagonist

  • Package size

    Bottle 30

  • Product code

    18403-1027

  • UPC

    068510178879

  • Generic name:

    buprenorphine hydrochloride and naloxone hydrochloride dihydrate

  • Brand reference:

    Suboxone®

  • Product code:

    18403-1027

  • Strength

    2mg/0.5mg

  • DIN

    02453908

  • UPC:

    068510178879

  • Therapeutic class

    Partial Opioid Agonist/Opioid Antagonist

  • Therapeutic area:

    Opiate Antagonist

  • Package size:

    Bottle 30

Composition

Active ingredient

buprenorphine hydrochloride and naloxone hydrochloride dihydrate


Non-medicinal ingredients

citric acid, crospovidone, lactose monohydrate, magnesium stearate, mannitol, natural & artificial lemon flavor, povidone, pregelatinized starch, sodium citrate, and sucralose

Product characteristics

  • Dosage form

    sublingual tablet

  • Shape

    round

  • Marking 1

    154

  • Marking 2

    -

  • Colour

    white to off-white

  • Secondary colour

    -

  • Scored

    -

  • Flavour

    -

  • Gluten

    currently not available

  • Latex

    currently not available

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

We're sorry, but this product monograph/consumer information leaflet is unavailable


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.