This brand name is authorized in Austria, Brazil, Canada, Cyprus, Germany, Ecuador, Estonia, Spain, Finland, France, Hong Kong, Croatia, Ireland, Israel, Italy, Lithuania, Malta, Mexico, Netherlands, Poland, Turkey, United States
The drug ANGELIQ 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
Drospirenone
UNII N295J34A25 - DROSPIRENONE
|
Drospirenone is a progestogen. In a therapeutic dosage, drospirenone also possesses antiandrogenic and mild antimineralocorticoid properties. It has no estrogenic, glucocorticoid and antiglucocorticoid activity. This gives drospirenone a pharmacological profile closely resembling the natural hormone progesterone. |
This drug has been classified in the anatomical therapeutic chemical (ATC) classification system as follows:
ATC code | Group title | Classification |
---|---|---|
G03FA17 | Drospirenone 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: BR | Câmara de Regulação do Mercado de Medicamentos | Identifier(s): 538901901112314 |
Country: CA | Health Products and Food Branch | Identifier(s): 02268825 |
Country: DE | Bundesinstitut für Arzneimittel und Medizinprodukte | Identifier(s): 01689021 |
Country: EC | Agencia Nacional de Regulación, Control y Vigilancia Sanitaria | Identifier(s): 26.136-01-05 |
Country: EE | Ravimiamet | Identifier(s): 1165711, 1165722 |
Country: ES | Centro de información online de medicamentos de la AEMPS | Identifier(s): 65583 |
Country: FI | Lääkealan turvallisuus- ja kehittämiskeskus | Identifier(s): 015089 |
Country: FR | Base de données publique des médicaments | Identifier(s): 67172690 |
Country: HK | Department of Health Drug Office | Identifier(s): 53676 |
Country: HR | Agencija za lijekove i medicinske proizvode | Identifier(s): HR-H-410626445 |
Country: IE | Health Products Regulatory Authority | Identifier(s): 12463 |
Country: IL | מִשְׂרַד הַבְּרִיאוּת | Identifier(s): 4865 |
Country: IT | Agenzia del Farmaco | Identifier(s): 036170013 |
Country: LT | Valstybinė vaistų kontrolės tarnyba | Identifier(s): 1017736, 1017737, 1085696, 1087563 |
Country: MT | Medicines Authority | Identifier(s): MA639/01501 |
Country: MX | Comisión Federal para la Protección contra Riesgos Sanitarios | Identifier(s): 003M2005 |
Country: NL | Z-Index G-Standaard, PRK | Identifier(s): 117226 |
Country: PL | Rejestru Produktów Leczniczych | Identifier(s): 100137084 |
Country: TR | İlaç ve Tıbbi Cihaz Kurumu | Identifier(s): 8699546097494 |
Country: US | FDA, National Drug Code | Identifier(s): 50419-482, 50419-483 |
© All content on this website, including data entry, data processing, decision support tools, "RxReasoner" logo and graphics, is the intellectual property of RxReasoner and is protected by copyright laws. Unauthorized reproduction or distribution of any part of this content without explicit written permission from RxReasoner is strictly prohibited. Any third-party content used on this site is acknowledged and utilized under fair use principles.