PALEXIA SR tapentadol (as hydrochloride) 50 mg sustained release tablet blister pack Australien - Englisch - Department of Health (Therapeutic Goods Administration)

palexia sr tapentadol (as hydrochloride) 50 mg sustained release tablet blister pack

seqirus pty ltd - tapentadol hydrochloride, quantity: 58.24 mg (equivalent: tapentadol, qty 50 mg) - tablet, modified release - excipient ingredients: titanium dioxide; lactose monohydrate; propylene glycol; hypromellose; purified talc; colloidal anhydrous silica; macrogol 6000; microcrystalline cellulose; magnesium stearate - palexia sr is indicated for the management of severe pain where: ? other treatment options have failed, are contraindicated, not tolerated or are otherwise inappropriate to provide sufficient management of pain, and ? the pain is opioid-responsive, and ? requires daily, continuous, long-term treatment. palexia sr is not indicated for use in chronic non-cancer pain other than in exceptional circumstances. palexia sr is not indicated as an as-needed (prn) analgesia.

PALEXIA IR tapentadol (as hydrochloride) 100 mg tablet blister pack Australien - Englisch - Department of Health (Therapeutic Goods Administration)

palexia ir tapentadol (as hydrochloride) 100 mg tablet blister pack

seqirus pty ltd - tapentadol hydrochloride, quantity: 116.48 mg (equivalent: tapentadol, qty 100 mg) - tablet, film coated - excipient ingredients: croscarmellose sodium; magnesium stearate; lactose monohydrate; iron oxide yellow; purified talc; povidone; titanium dioxide; iron oxide red; polyvinyl alcohol; microcrystalline cellulose; macrogol 3350; iron oxide black - palexia 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.

PALEXIA IR tapentadol (as hydrochloride) 75 mg tablet blister pack Australien - Englisch - Department of Health (Therapeutic Goods Administration)

palexia ir tapentadol (as hydrochloride) 75 mg tablet blister pack

seqirus pty ltd - tapentadol hydrochloride, quantity: 87.36 mg (equivalent: tapentadol, qty 75 mg) - tablet, film coated - excipient ingredients: macrogol 3350; polyvinyl alcohol; iron oxide red; croscarmellose sodium; purified talc; lactose monohydrate; titanium dioxide; microcrystalline cellulose; povidone; magnesium stearate; iron oxide yellow - palexia 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.

PALEXIA IR tapentadol (as hydrochloride) 50 mg tablet blister pack Australien - Englisch - Department of Health (Therapeutic Goods Administration)

palexia ir tapentadol (as hydrochloride) 50 mg tablet blister pack

seqirus pty ltd - tapentadol hydrochloride, quantity: 58.24 mg (equivalent: tapentadol, qty 50 mg) - tablet, film coated - excipient ingredients: purified talc; titanium dioxide; croscarmellose sodium; polyvinyl alcohol; lactose monohydrate; macrogol 3350; microcrystalline cellulose; povidone; magnesium stearate - palexia 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.

Blackmores Multi Vitamins + Minerals Tablet Australien - Englisch - Department of Health (Therapeutic Goods Administration)

blackmores multi vitamins + minerals tablet

blackmores ltd - calcium pantothenate, quantity: 21.8 mg (equivalent: pantothenic acid, qty 20 mg); pyridoxine hydrochloride, quantity: 10 mg (equivalent: pyridoxine, qty 8.23 mg); ascorbic acid, quantity: 180 mg; manganese sulfate monohydrate, quantity: 6.16 mg (equivalent: manganese, qty 2 mg); biotin, quantity: 25 microgram; inositol, quantity: 25 mg; heavy magnesium oxide, quantity: 30.63 mg (equivalent: magnesium, qty 17.5 mg); zinc oxide, quantity: 6.2 mg (equivalent: zinc, qty 5 mg); folic acid, quantity: 200 microgram; calcium carbonate, quantity: 100 mg (equivalent: calcium, qty 40 mg); ferrous sulfate, quantity: 16 mg (equivalent: iron, qty 5 mg); choline bitartrate, quantity: 25 mg; d-alpha-tocopheryl acid succinate, quantity: 16.53 mg; potassium sulfate, quantity: 55.75 mg (equivalent: potassium, qty 25 mg); riboflavine, quantity: 8.5 mg; cyanocobalamin, quantity: 10 microgram; nicotinamide, quantity: 60 mg; thiamine nitrate, quantity: 7.5 mg; colecalciferol, quantity: 0.01 mg; retinol palmitate, quantity: 2.75 mg - tablet, film coated - excipient ingredients: microcrystalline cellulose; titanium dioxide; hypromellose; magnesium stearate; calcium hydrogen phosphate dihydrate; glycerol; iron oxide yellow; carnauba wax; hydrogenated vegetable oil; chlorophyllin-copper complex; sodium starch glycollate; maize starch; silicon dioxide; dl-alpha-tocopherol; sucrose; hydrolysed gelatin; hydrogenated soya oil; potable water; gelatin; butylated hydroxytoluene; aluminium starch octenylsuccinate; aluminium sodium silicate

ONDANSETRON TABLETS VIATRIS ondansetron (as hydrochloride dihydrate) 4 mg film-coated tablet blister pack Australien - Englisch - Department of Health (Therapeutic Goods Administration)

ondansetron tablets viatris ondansetron (as hydrochloride dihydrate) 4 mg film-coated tablet blister pack

dr reddys laboratories australia pty ltd - ondansetron hydrochloride dihydrate, quantity: 5 mg (equivalent: ondansetron, qty 4 mg) - tablet, film coated - excipient ingredients: microcrystalline cellulose; lactose monohydrate; magnesium stearate; pregelatinised maize starch; sodium starch glycollate; colloidal anhydrous silica; titanium dioxide; hypromellose; purified talc; iron oxide yellow; macrogol 400 - prevention and treatment of nausea and vomiting induced by cytotoxic therapy and radiotherapy.

ONDANSETRON TABLETS VIATRIS ondansetron (as hydrochloride dihydrate) 8 mg film-coated tablet blister pack Australien - Englisch - Department of Health (Therapeutic Goods Administration)

ondansetron tablets viatris ondansetron (as hydrochloride dihydrate) 8 mg film-coated tablet blister pack

dr reddys laboratories australia pty ltd - ondansetron hydrochloride dihydrate, quantity: 10 mg (equivalent: ondansetron, qty 8 mg) - tablet, film coated - excipient ingredients: lactose monohydrate; pregelatinised maize starch; magnesium stearate; colloidal anhydrous silica; microcrystalline cellulose; sodium starch glycollate; titanium dioxide; hypromellose; purified talc; iron oxide yellow; macrogol 400 - prevention and treatment of nausea and vomiting induced by cytotoxic therapy and radiotherapy.

BLACKMORES MULTIVITAMINS + MINERALS TABLET Australien - Englisch - Department of Health (Therapeutic Goods Administration)

blackmores multivitamins + minerals tablet

blackmores ltd - zinc oxide, quantity: 6.2 mg (equivalent: zinc, qty 5 mg); riboflavine, quantity: 8.5 mg; nicotinamide, quantity: 60 mg; calcium pantothenate, quantity: 21.8 mg (equivalent: pantothenic acid, qty 20 mg); colecalciferol, quantity: 0.01 mg; d-alpha-tocopheryl acid succinate, quantity: 16.53 mg; ascorbic acid, quantity: 180 mg; pyridoxine hydrochloride, quantity: 10 mg; biotin, quantity: 25 microgram; cyanocobalamin, quantity: 10 microgram; folic acid, quantity: 200 microgram; choline bitartrate, quantity: 25 mg; inositol, quantity: 25 mg; retinol palmitate, quantity: 2.78 mg; calcium carbonate, quantity: 100 mg (equivalent: calcium, qty 40 mg); magnesium oxide, quantity: 30.63 mg (equivalent: magnesium, qty 17.5 mg); manganese sulfate monohydrate, quantity: 6.16 mg (equivalent: manganese, qty 2 mg); potassium sulfate, quantity: 55.75 mg (equivalent: potassium, qty 25 mg); thiamine nitrate, quantity: 7.5 mg; ferrous sulfate, quantity: 16 mg (equivalent: iron, qty 5 mg) - tablet, film coated - excipient ingredients: microcrystalline cellulose; calcium hydrogen phosphate; hydrogenated vegetable oil; magnesium stearate; sodium starch glycollate; chlorophyllin-copper complex; glycerol; iron oxide yellow; titanium dioxide; carnauba wax; hypromellose; maize starch; silicon dioxide; dl-alpha-tocopherol; sucrose; hydrolysed gelatin; hydrogenated soya oil; gelatin

Charmant Koala Kids Chewable Multivitamin Tablet Australien - Englisch - Department of Health (Therapeutic Goods Administration)

charmant koala kids chewable multivitamin tablet

south intraco pty ltd - ferrous fumarate, quantity: 3.04 mg (equivalent: iron, qty 1 mg); riboflavine, quantity: 1.2024 mg; nicotinamide, quantity: 13.4865 mg; zinc amino acid chelate, quantity: 1 mg (equivalent: zinc, qty 100 microgram); calcium pantothenate, quantity: 8.25 mg (equivalent: pantothenic acid, qty 7.4 mg); colecalciferol, quantity: 0.01 mg; d-alpha-tocopheryl acid succinate, quantity: 1.3 mg; ascorbic acid, quantity: 60 mg; pyridoxine hydrochloride, quantity: 1.0589 mg; biotin, quantity: 50 microgram; cyanocobalamin, quantity: 4.5 microgram; folic acid, quantity: 30 microgram; retinol palmitate, quantity: 1.375 mg; calcium hydrogen phosphate, quantity: 43 mg (equivalent: calcium, qty 10 mg); calcium carbonate, quantity: 9 mg (equivalent: calcium, qty 3.6 mg); copper gluconate, quantity: 42.86 microgram (equivalent: copper, qty 6 microgram); potassium sulfate, quantity: 4.46 mg (equivalent: potassium, qty 2 mg); thiamine nitrate, quantity: 1.0589 mg; magnesium carbonate hydrate, quantity: 10 mg (equivalent: magnesium, qty 2.5 mg) - tablet, film coated - excipient ingredients: sucralose; glucose; sodium cyclamate; saccharin sodium; fructose; stearic acid; colloidal anhydrous silica; magnesium stearate; calcium hydrogen phosphate; microcrystalline cellulose; maltodextrin; hypromellose; potable water; gelatin; butylated hydroxytoluene; aluminium starch octenylsuccinate; aluminium sodium silicate; sucrose; silicon dioxide; mono- and di- glycerides; maize starch; acacia; dl-alpha-tocopherol; medium chain triglycerides; flavour - for the maintenance & improvement of general well-being in kids. helps ensure children are getting essential vitamins and minerals needed for healthy growth and development.

AVSARTAN HCT 300/25 irbesartan 300 mg and hydrochlorothiazide 25 mg tablets blister pack Australien - Englisch - Department of Health (Therapeutic Goods Administration)

avsartan hct 300/25 irbesartan 300 mg and hydrochlorothiazide 25 mg tablets blister pack

arrotex pharmaceuticals pty ltd - hydrochlorothiazide, quantity: 25 mg; irbesartan, quantity: 300 mg - tablet, film coated - excipient ingredients: magnesium stearate; polysorbate 80; hypromellose; colloidal anhydrous silica; mannitol; sodium starch glycollate type b; povidone; titanium dioxide; iron oxide red; macrogol 3350; carnauba wax; iron oxide black - indicated for the treatment of hypertension. treatment should not be initiated with this fixed-dose combination.