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

noumed pharmaceuticals pty ltd - pseudoephedrine hydrochloride, quantity: 60 mg - tablet, uncoated - excipient ingredients: calcium hydrogen phosphate dihydrate; magnesium stearate; microcrystalline cellulose - fast temporary relief from a runny nose and reduce the swollen membranes of the nose and sinuses and helping breathe freely.

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

amdipharm mercury australia pty ltd - tranylcypromine sulfate, quantity: 13.68 mg (equivalent: tranylcypromine, qty 10 mg) - tablet, film coated - excipient ingredients: sucrose; erythrosine; magnesium stearate; gelatin; calcium sulfate dihydrate; maize starch; carnauba wax; titanium dioxide; hypromellose; propylene glycol; iron oxide yellow; iron oxide red; iron oxide black; cochineal - indications as at 5 october 1998: treatment of major depression.

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

proqualix pty ltd - in administration - diphenoxylate hydrochloride, quantity: 2.5 mg; atropine sulfate monohydrate, quantity: 0.025 mg; furazolidone, quantity: 50 mg - tablet - excipient ingredients: maize starch; lactose monohydrate; povidone; magnesium stearate - lomefen is indicated in diarrhoea caused by sensitive gram-positive and gram-negative organisms

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

mayne pharma international pty ltd - oxycodone hydrochloride, quantity: 5 mg - tablet - excipient ingredients: microcrystalline cellulose; sodium starch glycollate type a; silicon dioxide; lactose monohydrate; maize starch; stearic acid - mayne pharma oxycodone ir is indicated for the short-term management of severe pain for which other treatment options have failed, are contraindicated, not tolerated or are otherwise inappropriate to provide sufficient management of pain.

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

viatris pty ltd - oxycodone hydrochloride, quantity: 5 mg - tablet, uncoated - excipient ingredients: lactose; microcrystalline cellulose; stearic acid - endone is indicated for the short-term management of severe pain for which other treatment options have failed, are contraindicated, not tolerated or are otherwise inappropriate to provide sufficient management of pain.

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

viatris pty ltd - oxycodone hydrochloride, quantity: 5 mg - tablet, uncoated - excipient ingredients: lactose; microcrystalline cellulose; stearic acid - oxycodone viatris is indicated for the short-term management of severe pain for which other treatment options have failed, are contraindicated, not tolerated or are otherwise inappropriate to provide sufficient management of pain.

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

arrotex pharmaceuticals pty ltd - oxycodone hydrochloride, quantity: 5 mg - tablet, film coated - excipient ingredients: lactose monohydrate; sodium starch glycollate type a; magnesium stearate; microcrystalline cellulose; colloidal anhydrous silica; titanium dioxide; purified talc; polyvinyl alcohol; macrogol 3350; lecithin; brilliant scarlet 4r aluminium lake; indigo carmine aluminium lake - for the short-term management of severe pain for which other treatment options have failed, are contraindicated, not tolerated or are otherwise inappropriate to provide sufficient management of pain.

Kenya - English - Pharmacy and Poisons Board

cosmos limited rangwe road, off lunga lunga road, industrial - activated attapulgite bp and furazolidone bp - tablet - 350:100mg - other intestinal adsorbents

Philippines - English - FDA (Food And Drug Administration)

kramer pharma'l corp - furazolidone - tablet - 100mg

Philippines - English - FDA (Food And Drug Administration)

rilem pharma corp - furazolidone - tablet - 100mg