CO-DIOVAN

This brand name is authorized in Australia, Austria, Croatia, Cyprus, Estonia, Germany, Hong Kong SAR China, Ireland, Israel, Lithuania, Malta, Mexico, Netherlands, New Zealand, Nigeria, Poland, Singapore, South Africa, Spain, Turkey, UK.

Active ingredients

The drug CO-DIOVAN contains a combination of these active pharmaceutical ingredients (APIs):

1
UNII 80M03YXJ7I - VALSARTAN
 

Valsartan is an orally active, potent, and specific angiotensin II (Ang II) receptor antagonist. It acts selectively on the AT1-receptor subtype, which is responsible for the known actions of angiotensin II.

 
Read more about Valsartan
2
UNII 0J48LPH2TH - HYDROCHLOROTHIAZIDE
 

Hydrochlorothiazide is a diuretic with antihypertensive properties. It acts by inhibiting the renal tubular re-absorption of sodium and chloride ions, which are excreted with an accompanying volume of water. Potassium excretion is also promoted.

 
Read more about Hydrochlorothiazide

Medication package inserts

Below package inserts are available for further reading:

Document Type Information Source  
 CO-DIOVAN Film-coated tablet MPI, EU: SmPC Pharmaceutical Benefits Scheme (AU)

Medicine classification

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

ATC Group Classification
C09DA03 Valsartan and diuretics C Cardiovascular system → C09 Agents acting on the renin-angiotensin system → C09D Angiotensin II antagonists, combinations → C09DA Angiotensin II antagonists and diuretics
Discover more medicines within C09DA03

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 9372G, 9373H, 9374J, 9481B, 9482C
DE Bundesinstitut für Arzneimittel und Medizinprodukte 02428883, 02428966, 04460477, 04460566, 05030684, 05030690, 05030709, 08654698, 09493116, 10525979, 10525985, 10851578, 10851584, 11031587, 11080048, 11080054, 11367933, 11367962, 11367979, 11367985, 13510518, 15996519, 16234094, 16370124, 16370130, 16370147, 17267173
EE Ravimiamet 1031342, 1086016, 1086027, 1086038, 1086049, 1086050, 1086061, 1086072, 1086083, 1086094, 1086106, 1259827, 1259838, 1259849, 1259850, 1259861, 1259872, 1259883, 1259894, 1259906, 1259917, 1259928, 1259939, 1875225, 1875236, 1875247, 1875258, 1875269
ES Centro de información online de medicamentos de la AEMPS 034114215, 034114292, 62206, 65794, 66526, 69930, 69942
GB Medicines & Healthcare Products Regulatory Agency 138546, 142066, 142068, 142070, 161515, 161517, 180545, 76687, 76690, 81502
HK Department of Health Drug Office 43807, 49183, 59335, 59336, 59337, 59366, 59367
HR Agencija za lijekove i medicinske proizvode HR-H-035681755, HR-H-063837675, HR-H-133986302, HR-H-174157013, HR-H-819796318
IE Health Products Regulatory Authority 17442, 17913, 17985, 17992, 18705, 18708, 18709, 18710, 18727, 18728, 18729, 18735, 18750, 18751, 18752
IL מִשְׂרַד הַבְּרִיאוּת 4433, 4696, 4697
LT Valstybinė vaistų kontrolės tarnyba 1004719, 1004941, 1004942
MT Medicines Authority MA1249/02001, MA1249/02002, MA1249/02003, MA1249/02004, MA1249/02005, PI1438/03301A, PI1438/03302A, PI1438/03303A, PI908/04902A, PI908/04903A, PI908/04904A
MX Comisión Federal para la Protección contra Riesgos Sanitarios 355M98
NG Registered Drug Product Database 04-3691, A4-1503, A4-1787, B4-1425, B4-1426
Switch country to Nigeria in order to find specific presentations of CO-DIOVAN
NL Z-Index G-Standaard, PRK 50156, 71390, 77097, 85944, 85979
NZ Medicines and Medical Devices Safety Authority 10588, 10589, 12410, 12411, 8715
PL Rejestru Produktów Leczniczych 100123490
SG Health Sciences Authority 10538P, 11339P, 12011P
TR İlaç ve Tıbbi Cihaz Kurumu 8699504090406, 8699504090659, 8699504090970, 8699504091236, 8699504091243, 8699504091977, 8699504091984, 8699504091991
ZA Health Products Regulatory Authority 32/7.1.3/0336, 34/7.1.3/0441, 37/7.1.3/0225, 41/7.1.3/0148

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