DACEPTON

This brand name is authorized in Austria, Estonia, Spain, Finland, Ireland, Lithuania, Netherlands, Poland, Romania, United Kingdom

Active ingredients

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

1 Apomorphine
UNII F39049Y068 - APOMORPHINE HYDROCHLORIDE

Apomorphine is a direct stimulant of dopamine receptors and while possessing both D1 and D2 receptor agonist properties does not share transport or metabolic pathways with levodopa. Its actions on parkinsonian motor disability are likely to be mediated at post-synaptic receptor sites.

Read about Apomorphine

Medication package inserts

Below package inserts are available for further reading:

Title Information Source Document Type  
DACEPTON Solution for infusion Medicines & Healthcare Products Regulatory Agency (GB) MPI, EU: SmPC

Medicine classification

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

ATC code Group title Classification
N04BC07 Apomorphine N Nervous system → N04 Anti-parkinson drugs → N04B Dopaminergic agents → N04BC Dopamine agonists
Discover more medicines within N04BC07

Authorization and marketing

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

Country Identification scheme Identifier(s)
Country: EE Ravimiamet Identifier(s): 1548109, 1548110, 1548121, 1549223, 1549234, 1549245, 1549256, 1598160, 1598171, 1598182, 1598193
Country: ES Centro de información online de medicamentos de la AEMPS Identifier(s): 79174, 80998
Country: FI Lääkealan turvallisuus- ja kehittämiskeskus Identifier(s): 070119, 593776
Country: GB Medicines & Healthcare Products Regulatory Agency Identifier(s): 364369, 364372
Country: LT Valstybinė vaistų kontrolės tarnyba Identifier(s): 1051985, 1064574, 1064575, 1064576, 1064577, 1064578, 1064579, 1068361, 1072794, 1072795, 1072796, 1072797, 1072798, 1072799, 1081841
Country: NL Z-Index G-Standaard, PRK Identifier(s): 147044
Country: PL Rejestru Produktów Leczniczych Identifier(s): 100195851, 100329932, 100357851
Country: RO Agenția Națională a Medicamentului și a Dispozitivelor Medicale Identifier(s): W57967001, W57967002, W57967003, W57967004, W57967005, W57967006, W57967007, W60722001, W60722002, W60722003, W60722004, W60722005, W60722006, W63818001, W63818002, W63818003, W63818005, W63818006, W63818007

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