LUMIFY

This brand name is authorized in United States. It is also authorized in Canada.

Active ingredients

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

1
UNII 4S9CL2DY2H - BRIMONIDINE TARTRATE
 

Brimonidine is an alpha2-adrenergic receptor agonist that is 1000-fold more selective for the alpha2-adrenoceptor than the alpha1-adrenoreceptor. This selectivity results in no mydriasis and the absence of vasoconstriction in microvessels associated with human retinal xenografts.

 
Read more about Brimonidine

Medicine classification

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

ATC Group Classification
S01GA07 S Sensory organs → S01 Ophthalmologicals → S01G Decongestants and antiallergics → S01GA Sympathomimetics used as decongestants
Discover more medicines within S01GA07

Authorization and marketing

This drug has been assigned below unique identifiers within the countries it is being marketed:

Country Identification scheme Identifier(s)
CA Health Products and Food Branch 02517698
US FDA, National Drug Code 24208-537

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