Nya Zeeland - engelska - Medsafe (Medicines Safety Authority)

pharmacy retailing (nz) ltd t/a healthcare logistics - dexmedetomidine hydrochloride 0.1182 mg/ml equivalent to dexmedetomidine 0.1mg/ml - concentrate for injection - active: dexmedetomidine hydrochloride 0.1182 mg/ml equivalent to dexmedetomidine 0.1mg/ml excipient: sodium chloride water for injection - for sedation of initially intubated patients during treatment in an intensive care setting. the use of dexmedetomidine hydrochloride ever pharma by continuous intubation in these patents should not exceed 24 hours. for sedation of non-intubated patients prior to and/or during surgical and other procedures.

Malta - engelska - Medicines Authority

+pharma arzneimittel gmbh hafnerstrasse 211 8054 graz , austria - film-coated tablet - vildagliptin 50 mg metformin hydrochloride 850 mg - drugs used in diabetes

Malta - engelska - Medicines Authority

+pharma arzneimittel gmbh hafnerstrasse 211 8054 graz , austria - film-coated tablet - metformin hydrochloride 1000 mg vildagliptin 50 mg - drugs used in diabetes

Australien - engelska - Department of Health (Therapeutic Goods Administration)

noumed pharmaceuticals pty ltd - ibuprofen, quantity: 400 mg - tablet, film coated - excipient ingredients: colloidal anhydrous silica; croscarmellose sodium; lactose monohydrate; hypromellose; macrogol 6000; sodium lauryl sulfate; microcrystalline cellulose; purified water; purified talc; povidone; stearic acid; titanium dioxide - for the temporary relief of pain and/or inflammation associated with headache, migraine headache, tension headache, neuralgia, muscular aches & pains, back pain, fibrositis, arthritis, oesteoarthritis, rheumatic pain, tennis elbow. toothache & dental pain, period pain, sinus pain, sore throat and cold & flu. reduces fever.

Australien - engelska - Department of Health (Therapeutic Goods Administration)

noumed pharmaceuticals pty ltd - doxylamine succinate, quantity: 25 mg - tablet, uncoated - excipient ingredients: microcrystalline cellulose; calcium hydrogen phosphate dihydrate; purified talc; pregelatinised maize starch; povidone; croscarmellose sodium; magnesium stearate - temporary relief of sleeplessness.

Australien - engelska - Department of Health (Therapeutic Goods Administration)

southern cross pharma pty ltd - terbinafine hydrochloride, quantity: 10 mg - cream - excipient ingredients: benzyl alcohol; polysorbate 60; purified water; sorbitan monostearate; sodium hydroxide; cetyl alcohol; stearyl alcohol; isopropyl myristate; cetyl palmitate - treatment of ringworm (tinea corporis, tinea cruris and tinea pedis) caused by dermatophytes such as trichophyton (e.g. t. rubrum, t. mentagrophytes, t. verrucosum, t. violaceum), microsporum canis, and epidermophyton floccosum.,cutaneous candidiasis

Egypten - engelska - EDA (Egyptian Drug Authority)

pharma medica-egypt - eye drops - 10 mg/ml

Australien - engelska - Department of Health (Therapeutic Goods Administration)

arrotex pharmaceuticals pty ltd - paracetamol, quantity: 665 mg - tablet, modified release - excipient ingredients: colloidal anhydrous silica; povidone; sodium starch glycollate type a; microcrystalline cellulose; magnesium stearate; titanium dioxide; purified talc; macrogol 6000; maize starch; pregelatinised maize starch; hypromellose - effective for the relief of persistent pain associated with osteoarthritis and muscle aches and pains such as backache. pharmacy choice osteo relief paracetamol 665 mg also provides effective, temporary relief of pain and discomfort associated with headache, tension headache, period pain, toothache and pain after dental procedures, and cold and flu. reduces fever.

Australien - engelska - Department of Health (Therapeutic Goods Administration)

pharmacor pty ltd - olanzapine, quantity: 5 mg - tablet, film coated - excipient ingredients: pectin; mannitol; isopropyl alcohol; hyprolose; purified talc; lactose monohydrate; purified water; triacetin; titanium dioxide; magnesium stearate; propylene glycol; butan-1-ol; strong ammonia solution; iron oxide black; ethanol; shellac; sulfuric acid - olanzapine is indicated for the treatment of schizophrenia and related psychoses.,olanzapine alone or in combination with lithium or valproate is indicated for the short-term treatment of acute manic episodes associated with bipolar i disorder.,olanzapine is indicated for preventing recurrence of manic, mixed or depressive episodes in bipolar i disorder.

Australien - engelska - Department of Health (Therapeutic Goods Administration)

pharmacor pty ltd - olanzapine, quantity: 10 mg - tablet, film coated - excipient ingredients: purified water; lactose monohydrate; titanium dioxide; isopropyl alcohol; pectin; magnesium stearate; triacetin; hyprolose; purified talc; mannitol; propylene glycol; butan-1-ol; strong ammonia solution; iron oxide black; ethanol; shellac; sulfuric acid - olanzapine is indicated for the treatment of schizophrenia and related psychoses.,olanzapine alone or in combination with lithium or valproate is indicated for the short-term treatment of acute manic episodes associated with bipolar i disorder.,olanzapine is indicated for preventing recurrence of manic, mixed or depressive episodes in bipolar i disorder.