MENACTRA

This brand name is authorized in United States. It is also authorized in Brazil, Canada, Ecuador, Hong Kong SAR China, Israel, Japan, New Zealand, Nigeria, Singapore, South Africa, Tunisia, Turkey.

Active ingredients

The drug MENACTRA contains a combination of these active pharmaceutical ingredients (APIs):

1
UNII 1I86B47NY4 - NEISSERIA MENINGITIDIS GROUP A CAPSULAR POLYSACCHARIDE ANTIGEN
 
Read more about Meningococcal serogroup A polysaccharide vaccine
2
UNII 9B7N7Y96MK - NEISSERIA MENINGITIDIS GROUP C (STRAIN C11) OLIGOSACCHARIDE CRM-197 ADIPIC ACID CONJUGATE
 
Read more about Meningococcal serogroup C polysaccharide vaccine
3
UNII 9F8QQ6EER1 - NEISSERIA MENINGITIDIS GROUP W-135 CAPSULAR POLYSACCHARIDE ANTIGEN
 
Read more about Meningococcal serogroup W135 polysaccharide vaccine
4
UNII CBZ4BH7TJ1 - NEISSERIA MENINGITIDIS GROUP Y CAPSULAR POLYSACCHARIDE ANTIGEN
 
Read more about Meningococcal serogroup Y polysaccharide vaccine

Medicine classification

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

ATC Group Classification
J07AH Meningococcal vaccines J Antiinfectives for systemic use → J07 Vaccines → J07A Bacterial vaccines
Discover more medicines within J07AH

Authorization and marketing

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

Country Identification scheme Identifier(s)
BR Câmara de Regulação do Mercado de Medicamentos 576720060072017, 576720060072117
CA Health Products and Food Branch 02279924
EC Agencia Nacional de Regulación, Control y Vigilancia Sanitaria 30167-04-12
HK Department of Health Drug Office 60659
IL מִשְׂרַד הַבְּרִיאוּת 7485
JP 医薬品医療機器総合機構 6311401A1023
NG Registered Drug Product Database A6-0407
Switch country to Nigeria in order to find specific presentations of MENACTRA
NZ Medicines and Medical Devices Safety Authority 15192
SG Health Sciences Authority 13922P
TN Direction de la Pharmacie et du Médicament 16543011
TR İlaç ve Tıbbi Cihaz Kurumu 8699625960503, 8699625960510
US FDA, National Drug Code 49281-589
ZA Health Products Regulatory Authority 44/30.1/1064

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