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Subutex 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

Brand name

(ARTG)

: SUBUTEX buprenorphine 2mg (as hydrochloride) tablet blister pack

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)

Treatment of opiate dependence, including maintenance and detoxification, within a framework of medical, social and psychological treatment.

How to use this medicine

(ARTG)

This medicine contains one component only.

Component :

  • Tablet
  • Sublingual
  • Oval, flat, white to creamy white, glossy tablet with bevelled edges, debossed on one side with "B2".

Storage conditions

(ARTG)

  • Store below 30 degrees Celsius
  • Protect from Light
  • Protect from Moisture
  • Shelf lifetime is 3 Years.

Do I need a prescription ?

(ARTG)

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

  • 28 tablets pack
  • 7 tablets pack

Is this medicine subsidised ?

(PBS)

This medicine was verified as being available on the PBS (Pharmaceutical Benefits Scheme) on November, 1 2024. To learn more about this subsidy, visit the Pharmaceutical Benefits Scheme (PBS) website.

Pregnant or planning a pregnancy ?

(AHT)

For the active ingredient buprenorphine

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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