RIGEVIDON

This brand name is authorized in Austria, Ecuador, Spain, Finland, Hong Kong, Lithuania, Poland, Romania, United Kingdom

Active ingredients

The drug RIGEVIDON contains a combination of these active pharmaceutical ingredients (APIs):

1 17 alpha-Ethinylestradiol
UNII 423D2T571U - ETHINYL ESTRADIOL

Ethinylestradiol is chemically and biologically identical to endogenous human oestradiol. It substitutes for the loss of estrogen production in menopausal women, and alleviates menopausal symptoms. Estrogens prevent bone loss following menopause or ovariectomy.

Read about 17 alpha-Ethinylestradiol
2 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  
RIGEVIDON Coated tablet Web Search 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
G03AA07 Levonorgestrel and ethinylestradiol G Genito urinary system and sex hormones → G03 Sex hormones and modulators of the genital system → G03A Hormonal contraceptives for systemic use → G03AA Progestogens and estrogens, fixed combinations
Discover more medicines within G03AA07

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): 26.633-10-05
Country: ES Centro de información online de medicamentos de la AEMPS Identifier(s): 68970
Country: FI Lääkealan turvallisuus- ja kehittämiskeskus Identifier(s): 090327
Country: GB Medicines & Healthcare Products Regulatory Agency Identifier(s): 173468
Country: HK Department of Health Drug Office Identifier(s): 45789
Country: LT Valstybinė vaistų kontrolės tarnyba Identifier(s): 1012317, 1012318, 1074198, 1080875
Country: PL Rejestru Produktów Leczniczych Identifier(s): 100101465, 100298806, 100410628, 100410835
Country: RO Agenția Națională a Medicamentului și a Dispozitivelor Medicale Identifier(s): W01969001, W01969002

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