AFRABRON

This brand name is authorized in Nigeria.

Active ingredients

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

1
UNII UM5219H89V - IRON POLYMALTOSE
 
Read more about Iron polymaltose

Packages

This drug has been approved in Nigeria as follows:

Identifier Form Presentation Description Approval
A11-100077 Syrup Afrabron Syrup SYRUP 50 mg/5 mL 1 x 200 mL Syrup Orange Flavored Syrup 17/05/2021

Medicine classification

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

ATC Group Classification
B03AE10 Various combinations B Blood and blood forming organs → B03 Antianemic preparations → B03A Iron preparations → B03AE Iron in other combinations
Discover more medicines within B03AE10

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 A11-100077

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