NECOTRIM

This brand name is authorized in Nigeria.

Active ingredients

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

1
UNII JE42381TNV - SULFAMETHOXAZOLE
 

Sulfamethoxazole competitively inhibits the utilisation of para-aminobenzoic acid in the synthesis of dihydrofolate by the bacterial cell resulting in bacteriostasis.

 
Read more about Sulfamethoxazole
2
UNII AN164J8Y0X - TRIMETHOPRIM
 

Trimethoprim is a dihydrofolate reductase inhibitor, inhibiting the conversion of bacterial dihydrofolic acid to tetrahydrofolic acid, required for the synthesis of some amino acids. Its effects are considerably greater on the cells of micro-organisms than on the mammalian cells.

 
Read more about Trimethoprim

Packages

This drug has been approved in Nigeria as follows:

Identifier Form Presentation Description Approval
04-2377 Suspension Necotrim SUSP 200 mg/5 mL; 40mg/5 mL Each 5 mL suspension contains: Sulfamethoxazole 200 mg, Trimethoprim 40 mg 29/03/2021
A11-100053 Tablet Necotrim 960 mg Tablet TAB 800 mg; 160 mg Each tablet contains: Sulfamethoxazole 800 mg, Trimethoprim 160 mg 29/03/2021

Medicine classification

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

ATC Group Classification
J01EE01 Sulfamethoxazole and trimethoprim J Antiinfectives for systemic use → J01 Antibacterials for systemic use → J01E Sulfonamides and trimethoprim → J01EE Combinations of sulfonamides and trimethoprim, incl. derivatives
Discover more medicines within J01EE01

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 04-2377, A11-100053

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