Marketed in 54 countries across Europe, the Americas, Asia-Pacific, and parts of North Africa, Actos is a globally distributed brand of pioglitazone hydrochloride, classified within the category of hypoglycemic drugs used in diabetes. Its broad regulatory footprint means travellers, expatriates, and family members managing long-term diabetes therapy frequently encounter the same medication in unfamiliar pharmacies abroad.
Actos is prescribed in the management of type 2 diabetes mellitus, generally as part of a longer-term plan that also addresses lifestyle factors and may sit alongside other glucose-lowering medications. The structured indication list further down this page details the registered uses recognised by national regulators in the markets where Actos is sold.
Because Actos is registered in so many countries — among them Canada, Australia, China, Egypt, Argentina, and the Czech Republic — international readers often see it under the Actos name in one country and under a different commercial label or as a generic in the next. Brand naming conventions, packaging, and prescription pathways vary considerably between regulatory regimes, and a pharmacist working in the destination country is usually the most efficient person to confirm whether a pioglitazone-containing product is the appropriate equivalent of what was originally prescribed back home.
Other medications used in the management of type 2 diabetes — both within the same hypoglycemic class and in adjacent classes — circulate worldwide under a wide range of molecules and brand names, and not all are interchangeable with pioglitazone. Decisions about starting, stopping, or switching any diabetes medication belong with a clinician who knows the patient's full history, and a local pharmacist can support that conversation by clarifying what is available regionally.
Shelf life
3 years.
Date of revision of the text
26/05/2016
Marketing authorisation holder
Takeda Pharma A/S
Dybendal Alle 10,
DK-2630 Taastrup
Denmark
Special precautions for storage
This medicinal product does not require any special storage conditions.
Nature and contents of container
Aluminium/aluminium blisters, packs of 14, 28, 30, 50, 56, 84, 90, 98, 112 and 196 tablets.
Not all pack sizes may be marketed.
Marketing authorisation number(s)
EU/1/00/150/001
EU/1/00/150/002
EU/1/00/150/003
EU/1/00/150/004
EU/1/00/150/005
EU/1/00/150/006
EU/1/00/150/007
EU/1/00/150/008
EU/1/00/150/009
EU/1/00/150/010
EU/1/00/150/011
EU/1/00/150/012
EU/1/00/150/013
EU/1/00/150/014
EU/1/00/150/015
EU/1/00/150/016
EU/1/00/150/017
EU/1/00/150/018
EU/1/00/150/019
EU/1/00/150/020
EU/1/00/150/021
EU/1/00/150/022
EU/1/00/150/023
EU/1/00/150/024
EU/1/00/150/025
EU/1/00/150/026
EU/1/00/150/027
EU/1/00/150/028
EU/1/00/150/029
EU/1/00/150/030
Special precautions for disposal and other handling
No special requirements for disposal.
Date of first authorisation/renewal of the authorisation
Date of first authorisation: 13/10/2000
Date of latest renewal: 31/08/2010