SAOTERM FORTE

This brand name is authorized in Nigeria.

Active ingredients

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

1
UNII C7D6T3H22J - ARTEMETHER
 

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.

 
Read more about Artemether
2
UNII F38R0JR742 - LUMEFANTRINE
 
Read more about Lumefantrine

Packages

This drug has been approved in Nigeria as follows:

Identifier Form Presentation Description Approval
A4-100564 Tablet SAOTERM FORTE TABLETS TAB 80 mg; 480 mg 1 X 6 58 NF-PP-304307 SAOTERM FORTE TABLETS ARTEMETHER 80MG +LUMEFANTRINE 480MG ARTEMETHER 80MG, LUMEFANTRINE 480MG, MICRO CRYSALLINE CELLULOSE, M.C.C.P (PH102, EXCIPIENTS: SODIUM LAURYL SULPHATE, PVPK-30, MAGNESIUM STEARATE, TALCUM, COLLOIDIAL SILICON DIOXIDE, CROSS POVIDONE COLOUR, PEDIMIX TARTRAZINE YELLOW, ISOPROPYL ALCOHOL, METHYLENE DICHLORIDE A4-100564 Drugs Imported Products 1x6tablets OTC 12/28/2022 SAOCO PHARMACEUTICAL LIMITED, 152 Awolowo Road, ikoyi 8023186153 saodrug@gmail.com KESAR PHARMA PVT. LTD, PLOT NO. 50 - P/2, AT BILESHWARPURA, CHHATRAL, TAL - KALOL DIST. GANDHINAGAR - 382729, GUJARAT STATE, INDIA. , India 31/10/2023

Medicine classification

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
Discover more medicines within P01BF01

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 A4-100564

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