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Suboxone 2/0.5 TM

You should seek medical advice in relation to medicines and use only as directed by a healthcare professional. Always read the label. If symptoms persist see your healthcare professional.

Active ingredients: buprenorphine + naloxone

Brand name

(ARTG)

: SUBOXONE FILM 2/0.5 buprenorphine (as hydrochloride) 2 mg/naloxone (as hydrochloride dihydrate) 0.5 mg soluble film sachet

Download the Consumer Medicine Information Leaflet

Download consumer medicine information leaflet (pdf) from the Therapeutic Goods Administration (TGA) website

What this medicine is used for

(ARTG)

For the treatment of opiate dependence within a framework of medical, social, and psychological treatment.

How to use this medicine

(ARTG)

This medicine contains one component only.

Component :

  • Soluble Film
  • Sublingual
  • Orange film imprinted with "N2" with white ink.

Storage conditions

(ARTG)

  • Store below 25 degrees Celsius
  • Shelf lifetime is 18 Months.

Do I need a prescription ?

(ARTG)

These medicines require authorisation for prescription from your doctor. It is Schedule 8 : Controlled Drug.

  • 28 sachets pack

Is this medicine subsidised ?

(PBS)

This medicine was verified as being available on the PBS (Pharmaceutical Benefits Scheme) on February, 1 2025. To learn more about this subsidy, visit the Pharmaceutical Benefits Scheme (PBS) website.

Pregnant or planning a pregnancy ?

(AHT)

For the active ingredient buprenorphine + naloxone

You should seek advice from your doctor or pharmacist about taking this medicine. They can help you balance the risks and the benefits of this medicine during pregnancy.

Reporting side effects

You can help ensure medicines are safe by reporting the side effects you experience.

You can report side effects to your doctor, or directly at www.tga.gov.au/reporting-problems

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