POSTINOR

This brand name is authorized in Austria, Brazil, Estonia, Finland, Hong Kong SAR China, Israel, Lithuania, Mexico, New Zealand, Nigeria, Romania, Singapore, Spain.

Active ingredients

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

1
UNII 5W7SIA7YZW - LEVONORGESTREL
 

The precise mode of action of levonorgestrel as an emergency contraceptive is not known. At the recommended regimen, levonorgestrel is thought to work mainly by preventing ovulation and fertilisation if intercourse has taken place in the preovulatory phase, when the likelihood of fertilisation is the highest.

 
Read more about Levonorgestrel

Medicine classification

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

ATC Group Classification
G03AC03 Levonorgestrel 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 G03AC03
G03AD01 Levonorgestrel G Genito urinary system and sex hormones → G03 Sex hormones and modulators of the genital system → G03A Hormonal contraceptives for systemic use → G03AD Emergency contraceptives
Discover more medicines within G03AD01

Authorization and marketing

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

Country Identification scheme Identifier(s)
BR Câmara de Regulação do Mercado de Medicamentos 568418010000017
EE Ravimiamet 1482803, 1816231
ES Centro de información online de medicamentos de la AEMPS 39664-9-6-2015, 67515, PL05276-0019
FI Lääkealan turvallisuus- ja kehittämiskeskus 104466, 449107
HK Department of Health Drug Office 49747
IL מִשְׂרַד הַבְּרִיאוּת 5165
LT Valstybinė vaistų kontrolės tarnyba 1011782, 1055255, 1066753, 1068230, 1092805
MX Comisión Federal para la Protección contra Riesgos Sanitarios 336M99
NG Registered Drug Product Database 04-6985
Switch country to Nigeria in order to find specific presentations of POSTINOR
NZ Medicines and Medical Devices Safety Authority 11656
RO Agenția Națională a Medicamentului și a Dispozitivelor Medicale W10117001, W68033001
SG Health Sciences Authority 11836P

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