Austràlia - anglès - Department of Health (Therapeutic Goods Administration)

juno pharmaceuticals pty ltd - pomalidomide, quantity: 3 mg - capsule, hard - excipient ingredients: pregelatinised starch; sodium stearylfumarate; mannitol; croscarmellose sodium; titanium dioxide; indigo carmine; purified water; iron oxide yellow; gelatin; propylene glycol; butan-1-ol; isopropyl alcohol; shellac; ethanol absolute; ammonia; potassium hydroxide - pomalidomide, in combination with bortezomib and dexamethasone, is indicated for the treatment of patients with relapsed or refractory multiple myeloma who have received at least one prior treatment regimen including lenalidomide.,pomalidomide, in combination with dexamethasone, is indicated for the treatment of patients with relapsed and refractory multiple myeloma who have received at least two prior treatment regimens, including both lenalidomide and bortezomib, and have demonstrated disease progression on the last therapy.

Austràlia - anglès - Department of Health (Therapeutic Goods Administration)

juno pharmaceuticals pty ltd - pomalidomide, quantity: 2 mg - capsule, hard - excipient ingredients: croscarmellose sodium; mannitol; sodium stearylfumarate; pregelatinised starch; titanium dioxide; indigo carmine; purified water; iron oxide yellow; erythrosine; gelatin; propylene glycol; butan-1-ol; isopropyl alcohol; shellac; ethanol absolute; ammonia; potassium hydroxide - pomalidomide, in combination with bortezomib and dexamethasone, is indicated for the treatment of patients with relapsed or refractory multiple myeloma who have received at least one prior treatment regimen including lenalidomide.,pomalidomide, in combination with dexamethasone, is indicated for the treatment of patients with relapsed and refractory multiple myeloma who have received at least two prior treatment regimens, including both lenalidomide and bortezomib, and have demonstrated disease progression on the last therapy.

Austràlia - anglès - Department of Health (Therapeutic Goods Administration)

juno pharmaceuticals pty ltd - pomalidomide, quantity: 4 mg - capsule, hard - excipient ingredients: pregelatinised starch; mannitol; sodium stearylfumarate; croscarmellose sodium; titanium dioxide; indigo carmine; purified water; gelatin; propylene glycol; butan-1-ol; isopropyl alcohol; shellac; ethanol absolute; ammonia; potassium hydroxide - pomalidomide, in combination with bortezomib and dexamethasone, is indicated for the treatment of patients with relapsed or refractory multiple myeloma who have received at least one prior treatment regimen including lenalidomide.,pomalidomide, in combination with dexamethasone, is indicated for the treatment of patients with relapsed and refractory multiple myeloma who have received at least two prior treatment regimens, including both lenalidomide and bortezomib, and have demonstrated disease progression on the last therapy.

Malàisia - anglès - NPRA (National Pharmaceutical Regulatory Agency, Bahagian Regulatori Farmasi Negara)

luen wah medical co. sdn. bhd. - favipiravir -

Austràlia - anglès - Department of Health (Therapeutic Goods Administration)

noumed pharmaceuticals pty ltd - pregabalin, quantity: 150 mg - capsule - excipient ingredients: purified talc; maize starch; pregelatinised maize starch; titanium dioxide; purified water; gelatin; sodium lauryl sulfate - noumed pregabalin (pregabalin) is indicated for the treatment of neuropathic pain in adults. noumed pregabalin (pregabalin) is indicated as adjunctive therapy in adults with partial seizures with or without secondary generalisation.

Austràlia - anglès - Department of Health (Therapeutic Goods Administration)

noumed pharmaceuticals pty ltd - pregabalin, quantity: 25 mg - capsule - excipient ingredients: purified talc; maize starch; pregelatinised maize starch; titanium dioxide; purified water; gelatin; sodium lauryl sulfate - noumed pregabalin (pregabalin) is indicated for the treatment of neuropathic pain in adults. noumed pregabalin (pregabalin) is indicated as adjunctive therapy in adults with partial seizures with or without secondary generalisation.

Estats Units - anglès - NLM (National Library of Medicine)

ningbo jiangbei ocean star trading co.,ltd - alcohol (unii: 3k9958v90m) (alcohol - unii:3k9958v90m), .alpha.-tocopherol acetate, dl- (unii: wr1wpi7ew8) (.alpha.-tocopherol, dl- - unii:7qwa1rio01), titanium dioxide (unii: 15fix9v2jp) (titanium dioxide - unii:15fix9v2jp) - uses: reduces bacteria on the skin. recommended for repeated use. directions: place enough product in your palm to thoroughly cover your hands. rub hands together briskly until dry.

Austràlia - anglès - APVMA (Australian Pesticides and Veterinary Medicines Authority)

amgrow pty ltd - petroleum oil - emulsion - oil in water - petroleum oil petroleum derivative-oil active 20.0 g/l - insecticide - citrus fruit (see label for exceptions) | grape | ornamental (see label) | pome fruit tree - established | rose | stone fruit or - aphid | black scale | citrus leafminer | grapevine scale | mealy bug | oystershell scale | pink scale | red scale | san jose' scale | scale | soft brown scale | spider mite | white wax scale | whitefly | citrus red scale | diaspidiotus ostreaeformis | diaspidiotus perniciosus | mealybug | quadraspidiotus perniciosus

Austràlia - anglès - APVMA (Australian Pesticides and Veterinary Medicines Authority)

aquatopia - formaldehyde(37mg/ml)+malachite green(0.32mg/ml) - topical solution/suspension - fungicide (fish) - fish aquarium freshwater | fish aquarium freshwater tropical | cold water | tropical - white spot | whitespot

Malta - anglès - Medicines Authority

beecham group plc 980 great west road, brentford, middlesex, tw8 9gs, united kingdom - white soft, paraffin, light liquid - cream - white soft paraffin 15 % (w/w) light liquid paraffin 6 % (w/w) - emollients and protectives