Australija - engleski - Department of Health (Therapeutic Goods Administration)

abbvie pty ltd - fluorometholone, quantity: 1 mg/ml - eye drops, suspension - excipient ingredients: benzalkonium chloride; disodium edetate; sodium chloride; monobasic sodium phosphate; dibasic sodium phosphate heptahydrate; polysorbate 80; sodium hydroxide; purified water; polyvinyl alcohol - indications as at 23 oct 1995 : for steroid responsive inflammation of the palpebral and bulbar conjunctiva, cornea and anterior segment of the globe.

Izrael - engleski - Ministry of Health

abbvie biopharmaceuticals ltd, israel - fluorometholone - ophthalmic suspension - fluorometholone 0.1 %w/v - fluorometholone - fluorometholone - to treat eye inflammation.

Novi Zeland - engleski - Medsafe (Medicines Safety Authority)

abbvie limited - 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

Kanada - engleski - Health Canada

sandoz canada incorporated - fluorometholone - suspension - 0.1% - fluorometholone 0.1% - corticosteroids

Australija - engleski - Department of Health (Therapeutic Goods Administration)

novartis pharmaceuticals australia pty ltd - fluorometholone acetate, quantity: 1 mg/ml - eye drops, suspension - excipient ingredients: sodium chloride; tyloxapol; benzalkonium chloride; monobasic sodium phosphate; hyetellose; purified water; hydrochloric acid; sodium hydroxide; disodium edetate - indications as at 21 april 1989: flurometholone acetate ophalmic suspension is indicated for use in the treatment of steroid responsive inflammatory conditions of the palpebral and bulbar conjunctiva, cornea, and anterior segment of the eye.

Novi Zeland - engleski - 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

Novi Zeland - engleski - Medsafe (Medicines Safety Authority)

novartis new zealand ltd - fluorometholone 0.1%{relative} (+5% overage) - eye drops, suspension - 0.1% w/v - active: fluorometholone 0.1%{relative} (+5% overage) excipient: benzalkonium chloride dibasic sodium phosphate disodium edetate dihydrate hydrochloric acid hypromellose monobasic sodium phosphate monohydrate polysorbate 80 polyvinyl alcohol purified water sodium chloride sodium hydroxide

Malta - engleski - Medicines Authority

novartis ireland limited vista building, elm park, merrion road, ballsbridge, dublin 4,, ireland - fluorometholone acetate - eye drops, suspension - fluorometholone acetate 1 mg/ml - ophthalmologicals

Velika Britanija - engleski - MHRA (Medicines & Healthcare Products Regulatory Agency)

abbvie ltd - fluorometholone - eye drops - 1mg/1ml

Irska - engleski - HPRA (Health Products Regulatory Authority)

allergan pharmaceuticals ireland - fluorometholone - eye drops, suspension - 0.1 percent weight/volume - corticosteroids, plain; fluorometholone