FEMOSTON

This brand name is authorized in Austria, Australia, Brazil, Cyprus, Germany, Estonia, Finland, Hong Kong, Croatia, Ireland, Israel, Lithuania, Malta, Netherlands, Poland, Romania, Singapore, United Kingdom, South Africa

Active ingredients

The drug FEMOSTON 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. Read about Estradiol

2 Dehydroprogesterone UNII 90I02KLE8K - DYDROGESTERONE

Dydrogesterone is an orally-active progestogen having an activity comparable to parenterally administered progesterone. Read about Dehydroprogesterone

Medication package inserts

Below package inserts are available for further reading:

Title	Information Source	Document Type
FEMOSTON Film-coated tablet	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
G03FA14	Dydrogesterone 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 G03FA14
G03FB08	Dydrogesterone 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
Discover more medicines within G03FB08

Authorization and marketing

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): 10142T, 10146B, 8244X
Country: BR	Câmara de Regulação do Mercado de Medicamentos	Identifier(s): 500214100032317, 500214100032417
Country: DE	Bundesinstitut für Arzneimittel und Medizinprodukte	Identifier(s): 00018419, 00056495, 00608925, 00608931, 00988709, 01020358, 01086133, 01086156, 01214789, 01214795, 03913439, 05023709, 06474704, 06901750, 06901767, 08603198, 08603206, 08737869, 09082494, 09082502, 10402797, 12381786, 12381792, 12415108, 16890562, 17165018, 17562972
Country: EE	Ravimiamet	Identifier(s): 1013803, 1082450, 1082528, 1082539, 1082540, 1375332, 1375343, 1375354
Country: FI	Lääkealan turvallisuus- ja kehittämiskeskus	Identifier(s): 004579, 024315, 058545, 402343
Country: GB	Medicines & Healthcare Products Regulatory Agency	Identifier(s): 142334, 161765, 161784, 182943, 185788, 186492, 212594, 25872, 33482, 33502, 374510, 376371, 381337, 390892, 396482, 396484, 398374
Country: HK	Department of Health Drug Office	Identifier(s): 40939, 49421, 49643
Country: HR	Agencija za lijekove i medicinske proizvode	Identifier(s): HR-H-056380101, HR-H-361841297, HR-H-663625220, HR-H-831928897
Country: IE	Health Products Regulatory Authority	Identifier(s): 24143, 24164, 34236, 36925
Country: IL	מִשְׂרַד הַבְּרִיאוּת	Identifier(s): 8388, 8659, 8660
Country: LT	Valstybinė vaistų kontrolės tarnyba	Identifier(s): 1003542, 1003544, 1015309, 1015311, 1055927, 1055928, 1055929
Country: MT	Medicines Authority	Identifier(s): MA1507/01101, MA1507/01102, MA1507/01103, MA1507/01104, PI1438/03401A, PI1438/03402A, PI1438/03403A, PI1438/03404A
Country: NL	Z-Index G-Standaard, PRK	Identifier(s): 101575, 104639, 111864, 96393
Country: PL	Rejestru Produktów Leczniczych	Identifier(s): 100111541, 100124147, 100169210, 100211930, 100231653, 100344943, 100349567, 100355160, 100366531, 100402451, 100413466, 100437076, 100455780, 100460842, 100462195, 100464909, 100466910
Country: RO	Agenția Națională a Medicamentului și a Dispozitivelor Medicale	Identifier(s): W69163001, W69163002
Country: SG	Health Sciences Authority	Identifier(s): 09530P, 11896P, 12121P
Country: ZA	Health Products Regulatory Authority	Identifier(s): 30/21.8.2/0256, 36/21.8.2/0329, 36/21.8.2/0330