RUPURUT
Chewable tablet, 500 mg
OTCActive license
Active substance (INN)
hydrotalcite
Pharmaceutical form
Pharmaceutical formChewable tablet
Strength500 mg
PackagingUkupno 50 tableta za žvakanje u blisteru (5x10) u kartonskoj kutiji
ManufacturerBayer Bitterfeld GmbH, Germany
Therapeutic groupAlimentary tract and metabolism (A02AD04)
Marketing authorization holder"EVROPA LEK PHARMA" DOO PODGORICA
Authorization dateDecember 9, 2024
Analogs in Montenegro
2Other medicines with the same active substance
Source: CInMED register