Teva-Oxycocet

  • Generic name

    oxycodone hydrochloride and acetaminophen

  • Brand reference

    Percocet®

  • Strength

    325 mg/5 mg

  • DIN

    00608165

  • Therapeutic class

    Opioid Analgesic

  • Therapeutic area

    Analgesics


  • Package size

    Bottle 500
    Bottle 100
    Blister 4 x 25

  • Product code

    65340-5670
    65340-5640
    65340-5641

  • UPC

    064589000561
    064589000554
    064589001933

  • Generic name:

    oxycodone hydrochloride and acetaminophen

  • Brand reference:

    Percocet®

  • Product code:

    65340-5670
    65340-5640
    65340-5641

  • Strength

    325 mg/5 mg

  • DIN

    00608165

  • UPC:

    064589000561
    064589000554
    064589001933

  • Therapeutic class

    Opioid Analgesic

  • Therapeutic area:

    Analgesics

  • Package size:

    Bottle 500
    Bottle 100
    Blister 4 x 25

Composition

Active ingredient

oxycodone hydrochloride and acetaminophen


Non-medicinal ingredients

colloidal silicon dioxide, crospovidone, magnesium stearate, microcrystalline cellulose, povidone, pregelatinized starch, sodium starch glycolate and stearic acid

Product characteristics

  • Dosage form

    tablet

  • Shape

  • Marking 1

    TEC

  • Marking 2

  • Colour

  • Secondary colour

    white

  • Scored

    yes

  • Flavour

  • Gluten

    no

  • 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.