Tsjekkia - tsjekkisk - SUKL (Státní ústav pro kontrolu léčiv)

vifor france, paris array - 2222 ŽelezitÁ sŮl polymaltosy; 644 kyselina listovÁ - Žvýkací tableta - 100mg/0,35mg - komplex Železa s isomaltosou a kyselina listovÁ

Slovakia - slovakisk - ŠÚKL (Štátny ústav pre kontrolu liečiv)

vifor france, francúzsko - Železo v kombinácii s kyselinou listovou - 12 - antianaemica

Tsjekkia - tsjekkisk - SUKL (Státní ústav pro kontrolu léčiv)

vifor france, paris array - 2222 ŽelezitÁ sŮl polymaltosy - sirup - 10mg/ml - komplex Železa s isomaltosou

Tsjekkia - tsjekkisk - SUKL (Státní ústav pro kontrolu léčiv)

vifor france, paris array - 2222 ŽelezitÁ sŮl polymaltosy - Žvýkací tableta - 100mg - komplex Železa s isomaltosou

Tsjekkia - tsjekkisk - SUKL (Státní ústav pro kontrolu léčiv)

vifor france, paris array - 2222 ŽelezitÁ sŮl polymaltosy - perorální kapky, roztok - 50mg/ml - komplex Železa s isomaltosou

Slovakia - slovakisk - ŠÚKL (Štátny ústav pre kontrolu liečiv)

vifor france, francúzsko - komplexy oxid železitý-polymaltóza - 12 - antianaemica

Slovakia - slovakisk - ŠÚKL (Štátny ústav pre kontrolu liečiv)

vifor france, francúzsko - komplexy oxid železitý-polymaltóza - 12 - antianaemica

Slovakia - slovakisk - ŠÚKL (Štátny ústav pre kontrolu liečiv)

vifor france, francúzsko - komplexy oxid železitý-polymaltóza - 12 - antianaemica

Australia - engelsk - Department of Health (Therapeutic Goods Administration)

aspen pharmacare australia pty ltd - iron polymaltose, quantity: 185 mg/ml (equivalent: iron, qty 50 mg/ml) - oral liquid - excipient ingredients: sodium propyl hydroxybenzoate; sodium methyl hydroxybenzoate; purified water; sucrose; sodium hydroxide; flavour - treatment of iron deficiency in adults and adolescents where the use of ferrous iron supplements is not tolerated, or otherwise inappropriate.,prevention of iron deficiency in adults and adolescents at high risk where the use of ferrous iron supplements is not tolerated, or otherwise inappropriate.

Australia - engelsk - Department of Health (Therapeutic Goods Administration)

aspen pharmacare australia pty ltd - iron polymaltose, quantity: 37 mg/ml (equivalent: iron, qty 10 mg/ml) - oral liquid - excipient ingredients: propyl hydroxybenzoate; purified water; sorbitol solution (70 per cent) (non-crystallising); ethanol; sucrose; sodium hydroxide; methyl hydroxybenzoate; flavour - treatment of iron deficiency in adults and adolescents where the use of ferrous iron supplements is not tolerated, or otherwise inappropriate. prevention of iron deficiency in adults and adolescents at high risk where the use of ferrous iron supplements is not tolerated, or otherwise inappropriate.