IMPLANON

This brand name is authorized in Australia, Austria, Brazil, Ecuador, Ireland, Malta, Mexico, Netherlands, New Zealand, Poland, Singapore, South Africa, Spain.

Active ingredients

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

1
UNII 304GTH6RNH - ETONOGESTREL
 

Etonogestrel is the biologically active metabolite of desogestrel, a progestagen widely used in OCs. It is structurally derived from 19-nortestosterone and binds with high affinity to progesterone receptors in the target organs. The contraceptive effect of etonogestrel is primarily achieved by inhibition of ovulation.

 
Read more about Etonogestrel

Medication package inserts

Below package inserts are available for further reading:

Document Type Information Source  
 IMPLANON NXT Implant for subdermal use MPI, EU: SmPC Health Products Regulatory Authority (IE)

Medicine classification

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

ATC Group Classification
G03AC08 Etonogestrel G Genito urinary system and sex hormones → G03 Sex hormones and modulators of the genital system → G03A Hormonal contraceptives for systemic use → G03AC Progestogens
Discover more medicines within G03AC08

Authorization and marketing

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

Country Identification scheme Identifier(s)
AU Pharmaceutical Benefits Scheme 8487Q
BR Câmara de Regulação do Mercado de Medicamentos 527301801154319, 527316110018803
EC Agencia Nacional de Regulación, Control y Vigilancia Sanitaria 29951-07-11
ES Centro de información online de medicamentos de la AEMPS 62628
IE Health Products Regulatory Authority 28801, 28853
MT Medicines Authority MA031/01701, PI770/08302A
MX Comisión Federal para la Protección contra Riesgos Sanitarios 321M2000
NL Z-Index G-Standaard 14266377
NL Z-Index G-Standaard, PRK 52353
NZ Medicines and Medical Devices Safety Authority 14189
PL Rejestru Produktów Leczniczych 100149791
SG Health Sciences Authority 14086P
ZA Health Products Regulatory Authority 34/18.8/0448

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