Israel - English - Ministry of Health

allergan israel ltd - bimatoprost - ophthalmic solution - bimatoprost 0.3 mg/ml - bimatoprost - bimatoprost - reduction of elevated intraocular pressure in chronic open angle glaucoma and ocular hypertension (as monotherapy or as adjunctive therapy to beta-blockers).

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

sanofi-aventis australia pty ltd - trimeprazine tartrate -

New Zealand - English - Medsafe (Medicines Safety Authority)

allergan new zealand ltd - dipivefrine hydrochloride 1 mg/ml (5% overage added) - eye drops, solution - 0.1 % - active: dipivefrine hydrochloride 1 mg/ml (5% overage added) excipient: benzalkonium chloride disodium edetate dihydrate hydrochloric acid purified water sodium chloride

New Zealand - English - Medsafe (Medicines Safety Authority)

allergan new zealand ltd - fluorometholone 1 mg/ml - eye drops, solution - 0.1% w/v - active: fluorometholone 1 mg/ml excipient: benzalkonium chloride dibasic sodium phosphate heptahydrate monobasic sodium phosphate monohydrate polysorbate 80 polyvinyl alcohol purified water sodium chloride sodium edetate sodium hydroxide

New Zealand - English - Medsafe (Medicines Safety Authority)

allergan new zealand ltd - levobunolol hydrochloride 0.25%{relative};   - eye drops, solution - 0.25 % - active: levobunolol hydrochloride 0.25%{relative}   excipient: benzalkonium chloride dibasic sodium phosphate heptahydrate disodium edetate dihydrate monobasic potassium phosphate polyvinyl alcohol purified water sodium chloride sodium hydroxide sodium metabisulfite

New Zealand - English - Medsafe (Medicines Safety Authority)

allergan new zealand ltd - levobunolol hydrochloride 0.5%;   - eye drops, solution - 0.5 % - active: levobunolol hydrochloride 0.5%   excipient: benzalkonium chloride dibasic sodium phosphate heptahydrate disodium edetate hydrochloric acid monobasic potassium phosphate polyvinyl alcohol purified water sodium chloride sodium metabisulfite

New Zealand - English - Medsafe (Medicines Safety Authority)

allergan new zealand ltd - prednisolone acetate 0.12% - eye drops, solution - 0.12 % - active: prednisolone acetate 0.12% excipient: benzalkonium chloride purified water sodium chloride

New Zealand - English - Medsafe (Medicines Safety Authority)

allergan new zealand ltd - prednisolone acetate 1% - eye drops, solution - 1 % - active: prednisolone acetate 1%

New Zealand - English - Medsafe (Medicines Safety Authority)

sanofi-aventis new zealand limited - alimemazine tartrate 0.6%{relative};  ; alimemazine tartrate 0.6%{relative} - syrup - 30 mg/5ml - active: alimemazine tartrate 0.6%{relative}   excipient: ascorbic acid citric acid as monohydrate ethanol prunus armeniaca purified water sodium benzoate sodium citrate dihydrate sodium metabisulfite sodium sulfite sucrose active: alimemazine tartrate 0.6%{relative} excipient: ascorbic acid citric acid monohydrate ethanol prunus armeniaca purified water sodium benzoate sodium citrate dihydrate sodium metabisulfite sodium sulfite sucrose - · urticaria

Malta - English - Medicines Authority

abbvie limited citywest business campus, dublin 24, ireland - powder for solution for injection - botulinum toxin type a 4 allergan units/0.1 millilitre - muscle relaxants