This brand name is authorized in Nigeria.
The drug ORTRIMEF contains a combination of these active pharmaceutical ingredients (APIs):
1
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UNII
C7D6T3H22J - ARTEMETHER
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Artemether is an antimalarial agent used to treat acute uncomplicated malaria. It is administered in combination with lumefantrine for improved efficacy. This combination therapy exerts its effects against the erythrocytic stages of Plasmodium spp. and may be used to treat infections caused by P. falciparum and unidentified Plasmodium species, including infections acquired in chloroquine-resistant areas. |
|
2
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UNII
F38R0JR742 - LUMEFANTRINE
|
This drug has been approved in Nigeria as follows:
Identifier | Form | Presentation | Description | Approval |
---|---|---|---|---|
A11-1287 | Tablet | Ortrimef 80/480 Tablets TAB 80 mg; 480 mg 1 X 8 | Ortrimef 80/480 Tablets A11-1287 Ortrimef ARTEMETHER, LUMEFANTRINE ANTIMALARIA ARTEMETHER 80MG, LUMEFANTRINE 480MG TABLETS 1 X 8 OVER THE COUNTER TREATMENT OF UNCOMPLICATED MALARIA CAUSED BY PLASMODIUM FALCIPARUM ORFEMA PHARMACEUTICAL INDUSTRY LIMITED NIGERIA ORFEMA PHARMACEUTICAL INDUSTRY LIMITED NIGERIA 08/25/2022 08/24/2027 | 25/08/2022 |
A4-9435 | Tablet | ORTRIMEF TABLET TAB 20 mg; 120 mg 1X24. 1X18, 1X12, 1X6 | RNW-PP-216504 ORTRIMEF TABLET A4-9435 ARTEMETER+LUMENFANTRINE Drugs 24 N/A 1X24. 1X18, 1X12, 1X6 TABLET ORFEMA PHARMACEUTICAL INDUSTRY LIMITED 14537852 info@orfema.com 5, ATILADE ADEBOWALE STREET, OFF DADDY SAVAGE ROAD, OFF IJU ROAD Nigeria ORFEMA PHARMACEUTICAL INDUSTRY LIMITED Renewal 8033265151 degunite2000@yahoo.com 5, ATILADE ADEBOWALE STREET, FAGBA – IJU, LAGOS STATE. 22/12/2023 20/12/2028 | 21/12/2023 |
This drug has been classified in the anatomical therapeutic chemical (ATC) classification system as follows:
ATC Group | Classification | |
---|---|---|
P01BF01 | Artemether and lumefantrine | 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 | A11-1287, A4-9435 |
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