MALACT

This brand name is authorized in Nigeria.

Active ingredients

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

1
UNII 6A9O50735X - ARTENIMOL
 

Artemisinin is used in the treatment of malaria due to species Plasmodium.

 
Read more about Artemisinin
2
UNII 854D7K8LXB - PIPERAQUINE PHOSPHATE
 
Read more about

Packages

This drug has been approved in Nigeria as follows:

Identifier Form Presentation Description Approval
A11-100073 Tablet Malact Tablet TAB 40 mg; 320 mg 186 Dihydroartemisinin 40 mg Piperaquine Phosphate 320 mg A11-100073 Malact Tablet Piperaquine Phosphate, Dihydroartemisinin, Croscarmelose Sodium, Lactose Monohydrate, Pregelatinized Starch, Hypromellose Cps, Magnesium Stearate, Opadry Blue F (Containing Hypromellose, Titanium Dioxide, Peg, Fd&C Blue Indigo Carmine Aluminum Lake, Iron Oxide Yellow) Antimalarial Oral 320 Mg, 40 Mg, 30 Mg, 27 Mg, 22 Mg, 2 Mg, 9 Mg, 16 mg Tablet Prescription Only Medicine (Pom) May And Baker Nigeria Plc May And Baker Nigeria Plc Nigeria 2021-03-30 2026-03-29 30/03/2021

Medicine classification

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

ATC Group Classification
P01BF07 P Antiparasitic products, insecticides and repellents → P01 Antiprotozoals → P01B Antimalarials → P01BF Artemisinin and derivatives, combinations
Discover more medicines within P01BF07

Authorization and marketing

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

Country Identification scheme Identifier(s)
NG Registered Drug Product Database A11-100073

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