This brand name is authorized in Austria, Australia, Brazil, Canada, Finland, New Zealand, Poland, South Africa
The drug ESTALIS contains a combination of these active pharmaceutical ingredients (APIs):
1
Estradiol
UNII CXY7B3Q98Z - ESTRADIOL HEMIHYDRATE
|
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. |
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. |
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 |
This drug has been assigned below unique identifiers within the countries it is being marketed:
Country | Identification scheme | Identifier(s) |
---|---|---|
Country: AU | Pharmaceutical Benefits Scheme | Identifier(s): 8427M, 8428N |
Country: BR | Câmara de Regulação do Mercado de Medicamentos | Identifier(s): 526505401172417 |
Country: CA | Health Products and Food Branch | Identifier(s): 02241835, 02241837 |
Country: FI | Lääkealan turvallisuus- ja kehittämiskeskus | Identifier(s): 575990 |
Country: NZ | Medicines and Medical Devices Safety Authority | Identifier(s): 10909, 10911 |
Country: PL | Rejestru Produktów Leczniczych | Identifier(s): 100096652, 100096669 |
Country: ZA | Health Products Regulatory Authority | Identifier(s): 37/21.8.2/0456, 37/21.8.2/0457 |
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