BIOMAG

This brand name is authorized in Nigeria.

Active ingredients

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

1	Magnesium silicate UNII C2E1CI501T - MAGNESIUM TRISILICATE
	Read more about Magnesium silicate
2	Aluminium hydroxide UNII 5QB0T2IUN0 - ALUMINUM HYDROXIDE
	Aluminium hydroxide is a slow-acting antacid. It is used to provide symptomatic relief in gastric hyperacidity. In addition, the antipeptic and demulcent activity of aluminium hydroxide helps to protect inflamed gastric mucosa against further irritation by gastric secretions.
	Read more about Aluminium hydroxide

Packages

This drug has been approved in Nigeria as follows:

Identifier	Form	Presentation	Description	Approval
A4-6609	Chewable tablet	Biomag Chewable Tablets TAB_CHEW 120 mg; 250 mg	BIOMAG CHEWABLE TABLETS A4-6609 BIOMAG Magnesium Trisilicate 250mg, Dried Aluminium Hydroxide 150mg, Peppermint flavour Antacid Tablet OTC Relief from heart burn, stomach ulcer and flatulence Bioraj Pharmaceuticals Limited No. 405, Kaiama Road, Ilorin, Kwara State Same as applicant Same as applicant 26/01/2023 25/01/2028	26/01/2023

Medicine classification

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

ATC Group		Classification
A02A	Antacids	A Alimentary tract and metabolism → A02 Drugs for acid related disorders
Discover more medicines within A02A

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	A4-6609