KLIOGEST

This brand name is authorized in Austria, Germany, Estonia, Finland, France, Hong Kong, Ireland, Lithuania, Netherlands, New Zealand, Poland, Turkey, South Africa

Active ingredients

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

1 Estradiol
UNII 4TI98Z838E - ESTRADIOL

Estradiol, is chemically and biologically identical to endogenous human estradiol. It substitutes for the loss of oestrogen production in menopausal women, and alleviates menopausal symptoms. Oestrogens prevent bone loss following menopause or ovariectomy.

Read about Estradiol
2 Norethisterone
UNII 9S44LIC7OJ - NORETHINDRONE ACETATE

Norethisterone has progestational actions similar to those of progesterone, but is a more potent inhibitor of ovulation and has weak oestrogenic and androgenic properties. It is used to treat a number of disorders of the menstrual cycle.

Read about Norethisterone

Medication package inserts

Below package inserts are available for further reading:

Title Information Source Document Type  
KLIOGEST Film-coated tablet Health Products Regulatory Authority (IE) 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
G03FA01 Norethisterone and estrogen G Genito urinary system and sex hormones → G03 Sex hormones and modulators of the genital system → G03F Progestogens and estrogens in combination → G03FA Progestogens and estrogens, fixed combinations
Discover more medicines within G03FA01

Authorization and marketing

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

Country Identification scheme Identifier(s)
Country: DE Bundesinstitut für Arzneimittel und Medizinprodukte Identifier(s): 07330373, 07330396, 07517077, 09423386, 09423392, 09442490
Country: EE Ravimiamet Identifier(s): 1030464, 1175453
Country: FI Lääkealan turvallisuus- ja kehittämiskeskus Identifier(s): 048270
Country: FR Base de données publique des médicaments Identifier(s): 68216773
Country: HK Department of Health Drug Office Identifier(s): 33931
Country: IE Health Products Regulatory Authority Identifier(s): 31283
Country: LT Valstybinė vaistų kontrolės tarnyba Identifier(s): 1001121, 1022045, 1085694
Country: NL Z-Index G-Standaard, PRK Identifier(s): 33448
Country: NZ Medicines and Medical Devices Safety Authority Identifier(s): 5204
Country: PL Rejestru Produktów Leczniczych Identifier(s): 100033539
Country: TR İlaç ve Tıbbi Cihaz Kurumu Identifier(s): 8699676090280
Country: ZA Health Products Regulatory Authority Identifier(s): Y/21.8.2/230

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