NOVOMIX-30

This brand name is authorized in Australia, Austria, Brazil, Canada, Cyprus, Estonia, Finland, France, Hong Kong SAR China, Ireland, Israel, Lithuania, Netherlands, New Zealand, Nigeria, Poland, Romania, Singapore, South Africa, Spain, Tunisia, Turkey, UK.

Active ingredients

The drug NOVOMIX-30 contains one active pharmaceutical ingredient (API):

1
UNII 978D8U419H - SACCHAROMYCES CEREVISIAE
 

The blood glucose lowering effect of insulin aspart is due to the facilitated uptake of glucose following binding of insulin to receptors on muscle and fat cells and to the simultaneous inhibition of glucose output from the liver. Insulin aspart produces a more rapid onset of action compared to soluble human insulin, together with a lower glucose concentration, as assessed within the first four hours after a meal. Insulin aspart has a shorter duration of action compared to soluble human insulin after subcutaneous injection.

 
Read more about Insulin aspart

Medicine classification

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

ATC Group Classification
A10AD05 Insulin aspart A Alimentary tract and metabolism → A10 Drugs used in diabetes → A10A Insulins and analogues → A10AD Insulins and analogues for injection, intermediate-acting combined with fast-acting
Discover more medicines within A10AD05

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 12238D, 8609D
BR Câmara de Regulação do Mercado de Medicamentos 526602001159415, 526602002155316
CA Health Products and Food Branch 02265435
EE Ravimiamet 1084788, 1084823, 1214468, 1214479, 1523786
ES Centro de información online de medicamentos de la AEMPS 00142009, 00142015, 00142021
FI Lääkealan turvallisuus- ja kehittämiskeskus 001490, 006024
FR Base de données publique des médicaments 61693569, 64239493, 67832552, 68182431
GB Medicines & Healthcare Products Regulatory Agency 143813, 143865, 201635, 32773, 32781, 376949, 376952, 379926
HK Department of Health Drug Office 52604, 61546
IE Health Products Regulatory Authority 64275, 68927, 68930, 76140
IL מִשְׂרַד הַבְּרִיאוּת 4621
LT Valstybinė vaistų kontrolės tarnyba 1004366, 1008620, 1029898, 1029899, 1059246, 1059247, 1059248
NG Registered Drug Product Database A6-0204
Switch country to Nigeria in order to find specific presentations of NOVOMIX-30
NL Z-Index G-Standaard 14719509, 14719517
NL Z-Index G-Standaard, PRK 121320, 121339, 121347, 65749
NZ Medicines and Medical Devices Safety Authority 10731, 9745
PL Rejestru Produktów Leczniczych 100102170, 100108906
RO Agenția Națională a Medicamentului și a Dispozitivelor Medicale W08254001, W08254002, W08973001, W08973002
SG Health Sciences Authority 12190P, 15480P
TN Direction de la Pharmacie et du Médicament 5993082
TR İlaç ve Tıbbi Cihaz Kurumu 8699676950690, 8699676950706
ZA Health Products Regulatory Authority 35/21.1/0031

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