NEXPLANON

This brand name is authorized in Canada, Estonia, Finland, France, Lithuania, Romania, Turkey, United Kingdom, United States

Active ingredients

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

1 Etonogestrel
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 about Etonogestrel

Medication package inserts

Below package inserts are available for further reading:

Title Information Source Document Type  
NEXPLANON Implant 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
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)
Country: CA Health Products and Food Branch Identifier(s): 02499509
Country: EE Ravimiamet Identifier(s): 1589171, 1657560
Country: FI Lääkealan turvallisuus- ja kehittämiskeskus Identifier(s): 097847
Country: FR Base de données publique des médicaments Identifier(s): 66845924
Country: GB Medicines & Healthcare Products Regulatory Agency Identifier(s): 180308, 381558
Country: LT Valstybinė vaistų kontrolės tarnyba Identifier(s): 1066966, 1073720
Country: RO Agenția Națională a Medicamentului și a Dispozitivelor Medicale Identifier(s): W68121001, W68121002
Country: TR İlaç ve Tıbbi Cihaz Kurumu Identifier(s): 8683280337299
Country: US FDA, National Drug Code Identifier(s): 0052-4330

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