Imdur 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
Brand name
(ARTG)
: IMDUR isosorbide mononitrate 120 mg modified release 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)
INDICATIONS AS AT 08 MAY 2001 : IMDUR DURULES are indicated for prophylactic treatment of angina pectoris. IMDUR DURULES are not recommended for the management of acute attacks of angina pectoris (see PRECAUTIONS).
How to use this medicine
(ARTG)
This medicine contains one component only.
Component :
- Tablet, modified release
- Oral
- a white to off-white, oval, biconvex, film-coated tablet with the engraving A/IF 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 tablets pack
- 7 (sample pack) pack
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
