FEMOSTON

This brand name is authorized in Austria, Australia, Brazil, Cyprus, Germany, Estonia, Finland, Hong Kong, 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: 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

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