Új-Zéland - angol - Medsafe (Medicines Safety Authority)

sandoz new zealand limited - calcium folinate pentahydrate 10.8 mg/ml (as 12.71 mg/ml of calcium folinate pentahydrate, equivalent to 10 mg/ml folinic acid) - concentrate for injection - 500 mg/50ml - active: calcium folinate pentahydrate 10.8 mg/ml (as 12.71 mg/ml of calcium folinate pentahydrate, equivalent to 10 mg/ml folinic acid) excipient: hydrochloric acid nitrogen sodium chloride sodium hydroxide water for injection - as rescue therapy to reduce toxicity following high-dose methotrexate therapy. has shown good results in the treatment of certain megaloblastic anaemias resulting from folic acid deficiency. this mainly occurs in infants, during pregnancy, in malabsorption syndromes, liver diseases, sprue and malnutrition. it is not more effective than folic acid for these conditions overdosage of methotrexate and in impaired methotrexate elimination reducing the toxicity and circumventing the effect of folic acid antagonists

Belgium - angol - AFMPS (Agence Fédérale des Médicaments et des Produits de Santé)

laboratoires s.m.b. sa-nv - calcium carbonate 2500 mg - eq. calcium 1000 mg; cholecalciferol 1000 iu - chewable tablet - 1000 mg - 1000 iu - calcium carbonate 2500 mg; cholecalciferol 1000 iu - calcium, combinations with vitamin d and/or other drugs

Belgium - angol - AFMPS (Agence Fédérale des Médicaments et des Produits de Santé)

sandoz sa-nv - calcium carbonate 2500 mg - eq. calcium 1000 mg; cholecalciferol 880 iu - eq. vitamin d3 0,022 mg - chewable tablet - 1000 mg - 880 iu - calcium carbonate 2500 mg; cholecalciferol 880 iu - calcium, combinations with vitamin d and/or other drugs

Írország - angol - HPRA (Health Products Regulatory Authority)

imbat limited - cholecalciferol; calcium carbonate - chewable tablet - 500mg/400iu mg/iu - calcium, combinations with vitamin d and/or other drugs

Ausztrália - angol - Department of Health (Therapeutic Goods Administration)

dr reddys laboratories australia pty ltd - calcium carbonate, quantity: 1.25 g (equivalent: calcium, qty 500 mg) - tablet, film coated - excipient ingredients: microcrystalline cellulose; crospovidone; croscarmellose sodium; povidone; magnesium stearate; hypromellose; macrogol 8000; chlorophyllin-copper complex; titanium dioxide; carnauba wax - for the treatment of: ? osteoporosis in select patients where vitamin d and calcium supplementation is recommended,prior to treatment, osteoporosis must be confirmed by: ? the finding of low bone mass of at least 2 standard deviations below the gender specific mean for young adults or by ? the presence of osteoporotic fracture

Írország - angol - HPRA (Health Products Regulatory Authority)

mylan ire healthcare limited - calcium carbonate; cholecalciferol - chewable tablet - 600/400iu base milligrams - calcium, combinations with vitamin d and/or other drugs

Belgium - angol - AFMPS (Agence Fédérale des Médicaments et des Produits de Santé)

theramex ireland ltd. - calcium carbonate 1250 mg - eq. calcium 500 mg; cholecalciferol concentrate powder form 20 mg - eq. cholecalciferol 2000 iu - chewable tablet - calcium, combinations with vitamin d and/or other drugs

Belgium - angol - AFMPS (Agence Fédérale des Médicaments et des Produits de Santé)

theramex ireland ltd. - calcium carbonate 1250 mg - eq. calcium 500 mg; cholecalciferol concentrate powder form 20 mg - eq. cholecalciferol 2000 iu - chewable tablet - calcium, combinations with vitamin d and/or other drugs

Írország - angol - HPRA (Health Products Regulatory Authority)

hermes arzneimittel gmbh - calcium carbonate cholecalciferol concentrate (powder form 100,000 iu/g) - tablets chewable - 1000/880

Új-Zéland - angol - Medsafe (Medicines Safety Authority)

inova pharmaceuticals (new zealand) limited - calcium carbonate 42.4 mg/ml; edetic acid 123.7 mg/ml; sodium hydroxide 33.9 mg/ml - solution for injection - 1g/5ml - active: calcium carbonate 42.4 mg/ml edetic acid 123.7 mg/ml sodium hydroxide 33.9 mg/ml excipient: water for injection