This brand name is authorized in Nigeria.
The drug MALACT contains a combination of these active pharmaceutical ingredients (APIs):
1
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UNII
6A9O50735X - ARTENIMOL
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Artemisinin is used in the treatment of malaria due to species Plasmodium. |
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2
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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 |
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 | |
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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