FUSIBACT

This brand name is authorized in Nigeria.

Active ingredients

The drug FUSIBACT contains one active pharmaceutical ingredient (API):

1
UNII J7P3696BCQ - FUSIDATE SODIUM
 

Fusidic acid belongs to a unique group of antibiotics, the fusidanes, which act to inhibit bacterial protein synthesis by blocking the lengthening of factor G. Fusidic acid is active against staphylococcus epidermidis and methicillin resistant staphylococci.

 
Read more about Fusidic acid

Packages

This drug has been approved in Nigeria as follows:

Identifier Form Presentation Description Approval
B4-8035 Cream FUSIBACT-B CREAM CREAM 0.1%; 2% 1x15g 50 RNW-PP-292833 FUSIBACT-B CREAM FUSIDIC ACID 2%W/W,BETHAMETASONE VALERATE 0.1%W/W Fusidic acid 20mg, betamethasonevalerate1.0mg,cream base B4-8035 Drugs Imported Products 1x15g Prescription Only Medicine (POM) 12/5/2022 ASSENE-LABOREX LIMITED, AMUWO ODOFIN INDUSTRIAL SCHEME LAGOS LAGOS 17769700 esther.amuzie@assene-laborex.com JAMJOOM PHARMA CO.LTD , PLOT NO MEI-3 PHASE V INDUSTRIAL CITY ,JEDDAH, SAUDI-ARABIA, Saudi Arabia 25/05/2023
B4-8036 Cream FUSIBACT CREAM CREAM 2% 115g 50 RNW-PP-305327 FUSIBACT CREAM SODUIM FUSIDATE 2%W/W Sodium fusidate 2%w/w B4-8036 Drugs Imported Products 115g Prescription Only Medicine (POM) 2/3/2023 ASSENE-LABOREX LIMITED, AMUWO ODOFIN INDUSTRIAL SCHEME LAGOS LAGOS 17769700 esther.amuzie@assene-laborex.com JAMJOOM PHARMA CO.LTD , PLOT NO MEI-3 PHASE V INDUSTRIAL CITY ,JEDDAH, SAUDI-ARABIA, Saudi Arabia 31/01/2024

Medicine classification

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

ATC Group Classification
D06AX01 Fusidic acid D Dermatologicals → D06 Antibiotics and chemotherapeutics for dermatological use → D06A Antibiotics for topical use → D06AX Other antibiotics for topical use
Discover more medicines within D06AX01

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 B4-8035, B4-8036

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