UTROGESTAN

This brand name is authorized in Australia, Austria, Brazil, Croatia, Cyprus, Ecuador, Estonia, France, Hong Kong SAR China, Ireland, Israel, Japan, Lithuania, Malta, Mexico, Netherlands, New Zealand, Poland, Romania, Singapore, South Africa, Spain, Tunisia, UK.

Active ingredients

The drug UTROGESTAN contains one active pharmaceutical ingredient (API):

1
UNII 4G7DS2Q64Y - PROGESTERONE
 

Progesterone is a natural progestogen, the main hormone of the corpus luteum and the placenta. It acts on the endometrium by converting the proliferating phase to the secretory phase.

 
Read more about Progesterone

Medication package inserts

Below package inserts are available for further reading:

Document Type Information Source  
 UTROGESTAN Capsule MPI, EU: SmPC Medicines & Healthcare Products Regulatory Agency (GB)

Medicine classification

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

ATC Group Classification
G03DA04 Progesterone G Genito urinary system and sex hormones → G03 Sex hormones and modulators of the genital system → G03D Progestogens → G03DA Pregnen (4) derivatives
Discover more medicines within G03DA04

Authorization and marketing

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

Country Identification scheme Identifier(s)
AU Pharmaceutical Benefits Scheme 10930G, 12598C
BR Câmara de Regulação do Mercado de Medicamentos 542213020000014, 542213020000114, 542215030000603
EC Agencia Nacional de Regulación, Control y Vigilancia Sanitaria 1581-MEE-1215, 1582-MEE-1215, 29625-02-11
EE Ravimiamet 1703944, 1781715, 1781726, 1809660, 1818671, 1823318, 1847370, 1847381, 1849877
ES Centro de información online de medicamentos de la AEMPS 60814, 64899
FR Base de données publique des médicaments 61673424, 63157698
GB Medicines & Healthcare Products Regulatory Agency 117590, 226768
HK Department of Health Drug Office 34020, 61091
HR Agencija za lijekove i medicinske proizvode HR-H-677297904, HR-H-957395225, HR-H-979088283
IE Health Products Regulatory Authority 58492
IL מִשְׂרַד הַבְּרִיאוּת 2902, 4728
JP 医薬品医療機器総合機構 2477700H1020
LT Valstybinė vaistų kontrolės tarnyba 1090521, 1090522
MT Medicines Authority MA727/00205, MA727/00501, PI1438/00701A, PI908/22301A
MX Comisión Federal para la Protección contra Riesgos Sanitarios 188M93
NL Z-Index G-Standaard, PRK 198366, 29181
NZ Medicines and Medical Devices Safety Authority 13679, 17513
PL Rejestru Produktów Leczniczych 100412142, 100458655, 100462951, 100468073, 100468731
RO Agenția Națională a Medicamentului și a Dispozitivelor Medicale W12320001, W42276001, W42276002, W42276003, W42276004
SG Health Sciences Authority 11437P, 15475P
TN Direction de la Pharmacie et du Médicament 5173031, 5173032
ZA Health Products Regulatory Authority 29/21.8.2/0215, A40/21.8.2/0771

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