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Monodur Durules 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)

: MONODUR isosorbide mononitrate 60 mg modified release 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)

INDICATIONS AS AT 08 MAY 2001: MONODUR is indicated for prophylactic treatment of angina pectoris. MONODUR is 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
  • Yellow biconvex, oval film-coated tablet scored on both sides, engraved A/ID 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 Schedule 4 : Prescription Only Medicine.

  • 15, 30 tablets 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

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