This brand name is authorized in Austria, Croatia, Cyprus, Estonia, France, Germany, Hong Kong SAR China, Ireland, Lithuania, Netherlands, New Zealand, Poland, Singapore, South Africa, Spain, Turkey, UK.
The drug TRISEQUENS contains a combination of these active pharmaceutical ingredients (APIs):
1
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UNII
CXY7B3Q98Z - ESTRADIOL HEMIHYDRATE
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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. |
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2
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UNII
9S44LIC7OJ - NORETHINDRONE ACETATE
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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. |
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This drug has been classified in the anatomical therapeutic chemical (ATC) classification system as follows:
| ATC Group | Classification | |
|---|---|---|
| G03FB05 | 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 → G03FB Progestogens and estrogens, sequential preparations |
This drug has been assigned below unique identifiers within the countries it is being marketed:
| Country | Identification scheme | Identifier(s) |
|---|---|---|
| DE | Bundesinstitut für Arzneimittel und Medizinprodukte | 01928997, 01929005 |
| EE | Ravimiamet | 1030453 |
| ES | Centro de información online de medicamentos de la AEMPS | 60706 |
| FR | Base de données publique des médicaments | 64725221 |
| GB | Medicines & Healthcare Products Regulatory Agency | 34496 |
| HK | Department of Health Drug Office | 33985 |
| HR | Agencija za lijekove i medicinske proizvode | HR-H-919057630 |
| IE | Health Products Regulatory Authority | 48844 |
| LT | Valstybinė vaistų kontrolės tarnyba | 1001920, 1085839 |
| NL | Z-Index G-Standaard, PRK | 30341 |
| NZ | Medicines and Medical Devices Safety Authority | 5202 |
| PL | Rejestru Produktów Leczniczych | 100068006, 100418825, 100431122 |
| SG | Health Sciences Authority | 06011P |
| TR | İlaç ve Tıbbi Cihaz Kurumu | 8699676090297 |
| ZA | Health Products Regulatory Authority | J/21.8.2/212 |
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