Pharmaceuticals - Community Register


Community register of medicinal products for human use


Product information

Invented name: Vipidia   
Auth. number : EU/1/13/844
Active substance : alogliptin
ATC: Anatomical main group: A - Alimentary tract and metabolism
Therapeutic subgroup: A10 - Drugs used in diabetes
Pharmacological subgroup: A10B - Blood glucose lowering drugs, excluding insulins
Chemical subgroup: A10BH - Dipeptidyl peptidase 4 (dpp-4) inhibitors
Chemical substance: A10BH04 - Alogliptin
(See WHO ATC Index)
Indication: Indicated in adults aged 18 years and older with type 2 diabetes mellitus to improve glycaemic control in combination with other glucose lowering medicinal products including insulin, when these, together with diet and exercise, do not provide adequate glycaemic control (see sections 4.4, 4.5 and 5.1 for available data on different combinations).
Marketing Authorisation Holder: Takeda Pharma A/S
Dybendal Alle 10, 2630 Taastrup, Danmark
EPAR and active package presentations

Package presentations

Information about presentations can be found in the website of the European Medicines Agency under the section "Product Information".
Likewise, presentations on which there has been a Commission decision are referred in the Summary of Product Characteristics (Annex I to the Commission Decision granting the marketing authorisation) which is available in the Community Register.

European Commission proceduresGoto top of the page

Close date procedure Procedure type EMEA number Decision summary publ decision docs annex
23/09/2013 Centralised - Authorisation EMEA/H/C/2182 (2013)6215 of 19/09/2013
25/04/2014 Centralised - Variation EMEA/H/C/2182/II/5
Updated with Decision(2015)231 of 15/01/2015
24/07/2014 Centralised - Variation EMEA/H/C/2182/II/1
Updated with Decision(2015)231 of 15/01/2015
24/07/2014 Centralised - Variation EMEA/H/C/2182/WS/520
Updated with Decision(2015)231 of 15/01/2015
21/11/2014 Centralised - Variation EMEA/H/C/2182/IAin/8/G
Updated with Decision(2015)231 of 15/01/2015
08/12/2014 Centralised - Variation EMEA/H/C/2182/IAin/9/G
19/01/2015 PSUSA - Modification EMEA/H/C/2182/PSUV/7 (2015)231 of 15/01/2015