DOPTELET

This brand name is authorized in United States. It is also authorized in Austria, Croatia, Estonia, Finland, Ireland, Lithuania, Poland, Romania, Spain, UK.

Active ingredients

The drug DOPTELET contains one active pharmaceutical ingredient (API):

1
UNII GDW7M2P1IS - AVATROMBOPAG MALEATE
 

Avatrombopag is an orally active, small molecule thrombopoietin (TPO) receptor agonist that stimulates proliferation and differentiation of megakaryocytes from bone marrow progenitor cells resulting in increased production of platelets. Avatrombopag does not compete with TPO for binding to the TPO receptor and has an additive effect with TPO on platelet production.

 
Read more about Avatrombopag

Medication package inserts

Below package inserts are available for further reading:

Document Type Information Source  
 DOPTELET Film-coated tablet MPI, US: SPL/PLR FDA, National Drug Code (US)
 DOPTELET Film-coated tablet MPI, EU: SmPC European Medicines Agency (EU)

Medicine classification

This drug has been classified in the anatomical therapeutic chemical (ATC) classification system as follows:

ATC Group Classification
B02BX08 B Blood and blood forming organs → B02 Antihemorrhagics → B02B Vitamin K and other hemostatics → B02BX Other systemic hemostatics
Discover more medicines within B02BX08

Authorization and marketing

This drug has been assigned below unique identifiers within the countries it is being marketed:

Country Identification scheme Identifier(s)
EE Ravimiamet 1798678, 1798689, 1888533
ES Centro de información online de medicamentos de la AEMPS 1191373
FI Lääkealan turvallisuus- ja kehittämiskeskus 113364, 498007, 556341
GB Medicines & Healthcare Products Regulatory Agency 388232, 388234, 393009
IE Health Products Regulatory Authority 89034, 89035, 89098
LT Valstybinė vaistų kontrolės tarnyba 1088088, 1088089, 1091786
PL Rejestru Produktów Leczniczych 100423565
RO Agenția Națională a Medicamentului și a Dispozitivelor Medicale W67183001, W67183002, W67183003
US FDA, National Drug Code 71369-020

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