PARIET

This brand name is authorized in Australia, Austria, Brazil, Canada, Cyprus, Finland, France, Germany, Hong Kong SAR China, Ireland, Italy, Japan, Lithuania, Malta, Mexico, Netherlands, Singapore, South Africa, Spain, Turkey, UK.

Active ingredients

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

1
UNII 3L36P16U4R - RABEPRAZOLE SODIUM
 

Rabeprazole belongs to the class of anti-secretory compounds, the substituted benzimidazoles, that do not exhibit anticholinergic or H2 histamine antagonist properties, but suppress gastric acid secretion by the specific inhibition of the H+/K+ -ATPase enzyme (the acid or proton pump).

 
Read more about Rabeprazole

Medication package inserts

Below package inserts are available for further reading:

Document Type Information Source  
 PARIET Gastro-resistant tablet 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
A02BC04 Rabeprazole A Alimentary tract and metabolism → A02 Drugs for acid related disorders → A02B DRUGS FOR PEPTIC ULCER AND GASTRO-OESOPHAGEAL REFLUX DISEASE (GORD) → A02BC Proton pump inhibitors
Discover more medicines within A02BC04

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 11670F, 12286P, 8507R, 8508T, 8509W
BR Câmara de Regulação do Mercado de Medicamentos 514503301118214, 514503304117219, 514503305113217, 514503306111218, 514512110026303, 514516020032203
CA Health Products and Food Branch 02243796, 02243797
DE Bundesinstitut für Arzneimittel und Medizinprodukte 00176578, 00176584, 00176590, 00176621, 00176638, 00176644, 03743339, 03743345, 13981904, 16206270
ES Centro de información online de medicamentos de la AEMPS 034216186-M, 039351010, 3400935514790, 355147-9, 355147-9IP, 62461, 62462
FI Lääkealan turvallisuus- ja kehittämiskeskus 065083, 108780, 378482, 514346, 551879, 557015, 568238
FR Base de données publique des médicaments 62909137, 66035518
GB Medicines & Healthcare Products Regulatory Agency 139447, 139449, 175884, 196973, 198588, 20088, 20094
HK Department of Health Drug Office 44935, 44936
IE Health Products Regulatory Authority 38811, 38825, 38868, 38920
IT Agenzia del Farmaco 034216022, 034216186
JP 医薬品医療機器総合機構 2329028F1023, 2329028F2020, 2329028F3026
LT Valstybinė vaistų kontrolės tarnyba 1021251, 1021252, 1021253, 1021254
MT Medicines Authority MA018/01901, MA018/01902, PI521/07404A, PI770/17301A, PI908/07701A, PI908/07702A
MX Comisión Federal para la Protección contra Riesgos Sanitarios 505M98
NL Z-Index G-Standaard, PRK 54860, 54879
SG Health Sciences Authority 11232P, 11233P, 15531P
TR İlaç ve Tıbbi Cihaz Kurumu 8699593045295
ZA Health Products Regulatory Authority 32/11.4.3/0614, 33/11.4.3/0206

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