TIE SURFACE CLEANER AND DISINFECTANT SPRAY Canada - English - Health Canada

tie surface cleaner and disinfectant spray

nitmoi labs inc - hypochlorous acid - spray - 0.017% - hypochlorous acid 0.017%

STEOVESS ONCE WEEKLY Ireland - English - HPRA (Health Products Regulatory Authority)

steovess once weekly

nycomed gmbh - sodium alendronate trihydrate (micronised) - tablets effervescent - 70 base milligrams

Fosamax New Zealand - English - Medsafe (Medicines Safety Authority)

fosamax

merck sharp & dohme (new zealand) limited - alendronate sodium trihydrate 13.05mg equivalent to 10 mg alendronic acid - tablet - 10 mg - active: alendronate sodium trihydrate 13.05mg equivalent to 10 mg alendronic acid excipient: croscarmellose sodium lactose magnesium stearate microcrystalline cellulose

Fosamax New Zealand - English - Medsafe (Medicines Safety Authority)

fosamax

merck sharp & dohme (new zealand) limited - alendronate sodium trihydrate 52.21mg equivalent to 40 mg alendronic acid - tablet - 40 mg - active: alendronate sodium trihydrate 52.21mg equivalent to 40 mg alendronic acid excipient: croscarmellose sodium lactose magnesium stearate microcrystalline cellulose - fosamax is indicated: · in postmenopausal women for the treatment of osteoporosis to prevent fractures, including those of the hip and spine (vertebral compression fractures). · in postmenopausal women who are at risk of developing osteoporosis fosamax is indicated for the prevention of osteoporosis to reduce the risk of future fracture. · for the treatment of osteoporosis in men to prevent fractures. · for the treatment and prevention of glucocorticoid-induced osteoporosis in men, premenopausal women and postmenopausal women receiving oestrogen. · for treatment of paget's disease of bone in men and women.

Fosamax New Zealand - English - Medsafe (Medicines Safety Authority)

fosamax

merck sharp & dohme (new zealand) limited - alendronate sodium trihydrate 6.53mg equivalent to 5 mg of alendronic acid - tablet - 5 mg - active: alendronate sodium trihydrate 6.53mg equivalent to 5 mg of alendronic acid excipient: croscarmellose sodium lactose magnesium stearate microcrystalline cellulose - fosamax is indicated: · in postmenopausal women for the treatment of osteoporosis to prevent fractures, including those of the hip and spine (vertebral compression fractures). · in postmenopausal women who are at risk of developing osteoporosis fosamax is indicated for the prevention of osteoporosis to reduce the risk of future fracture. · for the treatment of osteoporosis in men to prevent fractures. · for the treatment and prevention of glucocorticoid-induced osteoporosis in men, premenopausal women and postmenopausal women receiving oestrogen. · for treatment of paget's disease of bone in men and women.

Fosamax New Zealand - English - Medsafe (Medicines Safety Authority)

fosamax

organon (new zealand) limited - alendronate sodium trihydrate 91.37mg equivalent to 70 mg alendronic acid - tablet - 70 mg - active: alendronate sodium trihydrate 91.37mg equivalent to 70 mg alendronic acid excipient: croscarmellose sodium lactose magnesium stearate microcrystalline cellulose - fosamax is indicated: · in postmenopausal women for the treatment of osteoporosis to prevent fractures, including those of the hip and spine (vertebral compression fractures). · in postmenopausal women who are at risk of developing osteoporosis fosamax is indicated for the prevention of osteoporosis to reduce the risk of future fracture. · for the treatment of osteoporosis in men to prevent fractures. · for the treatment and prevention of glucocorticoid-induced osteoporosis in men, premenopausal women and postmenopausal women receiving oestrogen. · for treatment of paget's disease of bone in men and women.

Fosamax Plus New Zealand - English - Medsafe (Medicines Safety Authority)

fosamax plus

organon (new zealand) limited - alendronate sodium trihydrate 91.37mg equivalent to 70 mg alendronate anhydrous free acid; colecalciferol 140ug equivalent to 5600 iu;   - tablet - 70/140 - active: alendronate sodium trihydrate 91.37mg equivalent to 70 mg alendronate anhydrous free acid colecalciferol 140ug equivalent to 5600 iu   excipient: colloidal silicon dioxide croscarmellose sodium lactose magnesium stearate microcrystalline cellulose - fosamax plus is indicated for the treatment of osteoporosis in select patients where vitamin d supplementation is recommended.

Fosamax Plus New Zealand - English - Medsafe (Medicines Safety Authority)

fosamax plus

organon (new zealand) limited - alendronate sodium trihydrate 91.37mg equivalent to to 70 mg anhydrous free acid; colecalciferol 70ug equivalent to 2800 iu;   - tablet - 70/70 - active: alendronate sodium trihydrate 91.37mg equivalent to to 70 mg anhydrous free acid colecalciferol 70ug equivalent to 2800 iu   excipient: colloidal silicon dioxide croscarmellose sodium lactose magnesium stearate microcrystalline cellulose - fosamax plus is indicated for the treatment of osteoporosis in select patients where vitamin d supplementation is recommended.

Singulair New Zealand - English - Medsafe (Medicines Safety Authority)

singulair

merck sharp & dohme (new zealand) limited - montelukast sodium 4.16mg equivalent to 4 mg montelukast free acid - chewable tablet - 4 mg - active: montelukast sodium 4.16mg equivalent to 4 mg montelukast free acid excipient: aspartame cherry flavour 181612 croscarmellose sodium hyprolose iron oxide red magnesium stearate mannitol microcrystalline cellulose purified water - indicated in adult and paediatric patients 2 years of age and older for the prophylaxis and chronic treatment of asthma, including the prevention of day- and nighttime symptoms and the prevention of exercise-induced bronchospasm.

Singulair New Zealand - English - Medsafe (Medicines Safety Authority)

singulair

merck sharp & dohme (new zealand) limited - montelukast sodium 5.2mg equivalent to 5 mg montelukast free acid - chewable tablet - 5 mg - active: montelukast sodium 5.2mg equivalent to 5 mg montelukast free acid excipient: aspartame cherry flavour 181612 croscarmellose sodium hyprolose iron oxide red magnesium stearate mannitol microcrystalline cellulose - indicated in adult and paediatric patients 2 years of age and older for the prophylaxis and chronic treatment of asthma, including the prevention of day- and nighttime symptoms and the prevention of exercise-induced bronchospasm.