apo-travoprost solution
apotex inc - travoprost - solution - 0.003% - travoprost 0.003% - prostaglandin analogs
teva-travoprost z ophthalmic solution
teva canada limited - travoprost - solution - 0.004% - travoprost 0.004% - prostaglandin analogs
sandoz travoprost solution
sandoz canada incorporated - travoprost - solution - 0.004% - travoprost 0.004% - prostaglandin analogs
apo-travoprost z solution
apotex inc - travoprost - solution - 0.004% - travoprost 0.004% - prostaglandin analogs
pms-travoprost z solution
pharmascience inc - travoprost - solution - 0.004% - travoprost 0.004% - prostaglandin analogs
mylan-travoprost z solution
mylan pharmaceuticals ulc - travoprost - solution - 0.004% - travoprost 0.004% - prostaglandin analogs
duotrav travoprost 0.004% and timolol 0.5% (as maleate) eye drop solution bottle
novartis pharmaceuticals australia pty ltd - travoprost, quantity: 40 microgram/ml; timolol maleate, quantity: 6.8 mg/ml (equivalent: timolol, qty 5 mg/ml) - eye drops, solution - excipient ingredients: ethoxylated hydrogenated castor oil; sodium hydroxide; propylene glycol; hydrochloric acid; sodium chloride; mannitol; boric acid; purified water; polyquaternium-1 - duotrav is indicated for the reduction of elevated intraocular pressure in patients with open angle glaucoma or ocular hypertension for whom single agent therapy provides insufficient intraocular pressure reduction.
travatan z- travoprost solution/ drops
novartis pharmaceuticals corporation - travoprost (unii: wj68r08kx9) (travoprost - unii:wj68r08kx9) - travatan z® (travoprost ophthalmic solution) 0.004% is indicated for the reduction of elevated intraocular pressure (iop) in patients with open-angle glaucoma or ocular hypertension. none. risk summary there are no adequate and well-controlled studies in pregnant women to inform a drug-associated risk. in animal reproduction studies, subcutaneous (sc) administration of travoprost to pregnant mice and rats throughout the period of organogenesis produced embryo-fetal lethality, spontaneous abortion, and premature delivery at potentially clinically relevant doses. advise pregnant women of a potential risk to a fetus. because animal reproductive studies are not always predictive of human response, travatan z should be administered during pregnancy only if the potential benefit justifies the potential risk to the fetus. the background risk of major birth defects and miscarriage for the indicated population is unknown; however, in the u.s. general population, the estimated background risk of major birth defects is
travatan
novartis israel ltd - travoprost - ophthalmic solution - travoprost 0.004 %w/v - travoprost - travoprost - for the reduction of elevated intra ocular pressure in patients with open-angle glaucoma or ocular hypertension who are intolerant of other iop lowering medications or insufficiently responsive to another iop lowering medication.
travoprost sandoz 40mcg/ml eye drops solution
central procurement & supplies unit ub002 industrial estate, san gwann sgn 3000, malta - travoprost - eye drops, solution - travoprost 40 µg/ml - ophthalmologicals