LEVOSERT

This brand name is authorized in Austria, Ecuador, Estonia, Spain, Croatia, Ireland, Lithuania, Malta, New Zealand, Poland, United Kingdom

Active ingredients

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

1 Levonorgestrel
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 about Levonorgestrel

Medication package inserts

Below package inserts are available for further reading:

Title Information Source Document Type  
LEVOSERT Intrauterine delivery system (IUS) 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
G02BA03 Plastic IUD with progestogen G Genito urinary system and sex hormones → G02 Other gynecologicals → G02B Contraceptives for topical use → G02BA Intrauterine contraceptives
Discover more medicines within G02BA03

Authorization and marketing

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

Country Identification scheme Identifier(s)
Country: EC Agencia Nacional de Regulación, Control y Vigilancia Sanitaria Identifier(s): 6299-MEE-0621, 7705-MEE-1222
Country: EE Ravimiamet Identifier(s): 1500848
Country: ES Centro de información online de medicamentos de la AEMPS Identifier(s): 80021
Country: GB Medicines & Healthcare Products Regulatory Agency Identifier(s): 296643
Country: HR Agencija za lijekove i medicinske proizvode Identifier(s): HR-H-845986671, HR-H-896425945
Country: LT Valstybinė vaistų kontrolės tarnyba Identifier(s): 1057157
Country: MT Medicines Authority Identifier(s): MA1031/00401, MA1031/00402
Country: NZ Medicines and Medical Devices Safety Authority Identifier(s): 17592
Country: PL Rejestru Produktów Leczniczych Identifier(s): 100301320

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