BELARA

This brand name is authorized in Austria, Brazil, Croatia, Ecuador, Estonia, France, Hong Kong SAR China, Israel, Lithuania, Mexico, Poland, Romania, Singapore, Spain, Tunisia.

Active ingredients

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

1
UNII 0SY050L61N - CHLORMADINONE ACETATE
 
Read more about Chlormadinone
2
UNII 423D2T571U - ETHINYL ESTRADIOL
 

Ethinylestradiol is chemically and biologically identical to endogenous human oestradiol. It substitutes for the loss of estrogen production in menopausal women, and alleviates menopausal symptoms. Estrogens prevent bone loss following menopause or ovariectomy.

 
Read more about 17 alpha-Ethinylestradiol

Medicine classification

This drug has been classified in the anatomical therapeutic chemical (ATC) classification system as follows:

ATC Group Classification
G03AA15 Chlormadinone and ethinylestradiol G Genito urinary system and sex hormones → G03 Sex hormones and modulators of the genital system → G03A Hormonal contraceptives for systemic use → G03AA Progestogens and estrogens, fixed combinations
Discover more medicines within G03AA15

Authorization and marketing

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

Country Identification scheme Identifier(s)
BR Câmara de Regulação do Mercado de Medicamentos 542813120000018, 542817070001603, 542820010005607, 542820050007107
EC Agencia Nacional de Regulación, Control y Vigilancia Sanitaria 365210413, 4539-MEE-0119
EE Ravimiamet 1012880, 1094509, 1568279, 1568280, 1568291
ES Centro de información online de medicamentos de la AEMPS 21993, 5503487, 5503487IP, 5503487IP1, 66905, 71898
FR Base de données publique des médicaments 64875438
HK Department of Health Drug Office 65918
HR Agencija za lijekove i medicinske proizvode HR-H-368848654
IL מִשְׂרַד הַבְּרִיאוּת 4962, 4963
LT Valstybinė vaistų kontrolės tarnyba 1011517, 1011518, 1080503
MX Comisión Federal para la Protección contra Riesgos Sanitarios 082M2001
PL Rejestru Produktów Leczniczych 100323912, 100394160, 100403226, 100453499
RO Agenția Națională a Medicamentului și a Dispozitivelor Medicale W58349001, W58349002
SG Health Sciences Authority 14870P
TN Direction de la Pharmacie et du Médicament 6673121

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