Duride 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: isosorbide mononitrate
Pack: Duride 60 mg modified release tablet, 30, blister pack
Brand name
(ARTG)
: DURIDE Isosorbide mononitrate 60mg tablet blister packDownload 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)
Duride is indicated for the prophylactic treatment of angina pectoris. Duride is not recommended for the management of acute attacks of angina pectoris (see section 4.4 Special Warnings and Precautions for Use).
How to use this medicine
(ARTG)
This medicine contains one component only.
Component :
- Tablet, modified release
- Oral
- yellow, film coated, elliptical shaped tablet, 13. 1 x 7.1mm, scored on both sides and imprinted "IM I 60" on one side
Storage conditions
(ARTG)
- Store below 30 degrees Celsius
- Shelf lifetime is 3 Years.
Do I need a prescription ?
(ARTG)
These medicine packs are available from a pharmacist and requires a prescription. It is
- 30 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 isosorbide mononitrate
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
