Designation of Eltrombopag (Revolade) as an orphan drug - GlaxoSmithKline Australia

Administered by Department of Health, Disability and Ageing

Legislation au C2014G01841 In force Gazette

Legislation content

COMMONWEALTH OF AUSTRALIA

Department of Health
Therapeutic Goods Administration

THERAPEUTIC GOODS ACT 1989

 

DESIGNATION OF Eltrombopag (revolade) AS AN ORPHAN DRUG

 

I, Dr Anthony Gill, Delegate of the Secretary for the purposes of 16J of the Therapeutic Goods Regulations 1990 (“the Regulations”), acting under subregulation 16J(2) of the Regulations, designate Eltrombopag (REVOLADE) as an orphan drug on 29 October 2014 for the treatment of chronic idiopathic thrombocytopaenic purpura (ITP).

The dose form of Eltrombopag (REVOLADE) for this indication is powder for oral liquid.

The sponsor of Eltrombopag (REVOLADE) is GlaxoSmithKline Australia Pty ltd.

 

 

(Signed by)

 

Dr Anthony Gill

Delegate of the Secretary

29 October 2014

 

 

Interactions

Authorises

All Versions

Sourced from the Federal Register of Legislation at 26 August 2026. For the latest information on Australian Government law please go to https://www.legislation.gov.au.