MAGNEROT

This brand name is authorized in Germany, Lithuania, Romania.

Active ingredients

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

1
UNII VQ922CRY87 - MAGNESIUM OROTATE DIHYDRATE
 
Read more about Magnesium orotate

Medicine classification

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

ATC Group Classification
A12CC09 Magnesium orotate A Alimentary tract and metabolism → A12 Mineral supplements → A12C Other mineral supplements → A12CC Magnesium
Discover more medicines within A12CC09

Authorization and marketing

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

Country Identification scheme Identifier(s)
DE Bundesinstitut für Arzneimittel und Medizinprodukte 00150768, 00150774, 00150780, 00151147, 06963337, 06963343, 06963366
LT Valstybinė vaistų kontrolės tarnyba 1013146, 1013147
RO Agenția Națională a Medicamentului și a Dispozitivelor Medicale W04048001, W04048002, W04048003, W04048004, W04048005, W04048006, W04048007, W04048008

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