PHARMACY CHOICE IBUPROFEN DOUBLE STRENGTH ibuprofen 400 mg film-coated tablet blister pack Australia - Inggeris - Department of Health (Therapeutic Goods Administration)

pharmacy choice ibuprofen double strength ibuprofen 400 mg film-coated tablet blister pack

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.

PHARMACY ACTION PHARMISIL terbinafine hydrochloride 10 mg/g cream tube Australia - Inggeris - Department of Health (Therapeutic Goods Administration)

pharmacy action pharmisil terbinafine hydrochloride 10 mg/g cream tube

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

PHARMACY ACTION PARACETAMOL & IBUPROFEN film coated tablet blister pack Australia - Inggeris - Department of Health (Therapeutic Goods Administration)

pharmacy action paracetamol & ibuprofen film coated tablet blister pack

generic health pty ltd - ibuprofen, quantity: 200 mg; paracetamol, quantity: 500 mg - tablet, film coated - excipient ingredients: hypromellose; crospovidone; pregelatinised maize starch; titanium dioxide; microcrystalline cellulose; colloidal anhydrous silica; purified talc; magnesium stearate; povidone; purified water; polysorbate 80; polyvinyl alcohol; macrogol 3350; mica - temporary relief of acute (short term) pain and / or inflammation associated with headache, migraine headache, tension headache, sinus pain, toothache, dental procedures, backache, muscular aches and pains, period pain, sore throat, tennis elbow, rheumatic pain and arthritis, and the aches and pains associated with colds and flu. reduces fever.

Straben 8.75 mg lozenges Malta - Inggeris - Medicines Authority

straben 8.75 mg lozenges

uni-pharma kleon tsetis pharmaceutical laboratories s.a. 14th km national road athens - lamia 1, gr-145 64 kifissia, greece - lozenge - flurbiprofen 8.75 mg - throat preparations

Provist-Opto 5 mg/ml eye drops, solution in single-dose container Malta - Inggeris - Medicines Authority

provist-opto 5 mg/ml eye drops, solution in single-dose container

uni-pharma kleon tsetis pharmaceutical laboratories s.a. 14th km national road athens - lamia 1, gr-145 64 kifissia, greece - eye drops, solution - prednisolone 5 mg/ml - ophthalmologicals

OXAPROZIN- oxaprozin tablet Amerika Syarikat - Inggeris - NLM (National Library of Medicine)

oxaprozin- oxaprozin tablet

caraco pharmaceutical laboratories, ltd. - oxaprozin (unii: mhj80w9lrb) (oxaprozin - unii:mhj80w9lrb) - oxaprozin 600 mg - carefully consider the potential benefits and risks of oxaprozin tablet, usp and other treatment options before deciding to use oxaprozin tablet, usp. use the lowest effective dose for the shortest duration consistent with individual patient treatment goals (see warnings). oxaprozin tablet, usp is indicated: - for relief of the signs and symptoms of osteoarthritis - for relief of the signs and symptoms of rheumatoid arthritis - for relief of the signs and symptoms of juvenile rheumatoid arthritis oxaprozin tablet, usp is contraindicated in patients with known hyper-sensitivity to oxaprozin. oxaprozin tablet, usp should not be given to patients who have experienced asthma, urticaria, or allergic-type reactions after taking aspirin or other nsaids. severe, rarely fatal, anaphylactic-like reactions to nsaids have been reported in such patients (see warnings, anaphylactoid reactions and precautions, preexisting asthma). oxaprozin tablet, usp is contraindicated for the treatment of peri-operative pain in the setti

Sugammadex Pharmazac Solution for Injection 100mg/ml (2ml vial) Malta - Inggeris - Medicines Authority

sugammadex pharmazac solution for injection 100mg/ml (2ml vial)

pharmazac, s.a. 31 naousis str., 104 47, athens,, greece - sugammadex - solution for injection - sugammadex 200 mg - all other therapeutic products

Sugammadex Pharmazac Solution for Injection 100mg/ml (5ml vial) Malta - Inggeris - Medicines Authority

sugammadex pharmazac solution for injection 100mg/ml (5ml vial)

pharmazac, s.a. 31 naousis str., 104 47, athens,, greece - sugammadex - solution for injection - sugammadex 500 mg - all other therapeutic products

VELABINE vinorelbine (as tartrate) 30 mg soft capsules blister pack Australia - Inggeris - Department of Health (Therapeutic Goods Administration)

velabine vinorelbine (as tartrate) 30 mg soft capsules blister pack

luminarie pty ltd - vinorelbine tartrate, quantity: 41.55 mg (equivalent: vinorelbine, qty 30 mg) - capsule, soft - excipient ingredients: gelatin; partially dehydrated liquid sorbitol; polysorbate 80; macrogol 400; titanium dioxide; purified water; iron oxide red - non-small cell lung cancer: velabine is indicated for the first line treatment of advanced non-small cell lung cancer, as a single agent or in combination. ,breast cancer: velabine is indicated for the treatment of advanced breast cancer after failure of standard therapy as a single agent or in combination.

VELABINE vinorelbine (as tartrate) 20 mg soft capsules blister pack Australia - Inggeris - Department of Health (Therapeutic Goods Administration)

velabine vinorelbine (as tartrate) 20 mg soft capsules blister pack

luminarie pty ltd - vinorelbine tartrate, quantity: 27.7 mg (equivalent: vinorelbine, qty 20 mg) - capsule, soft - excipient ingredients: purified water; polysorbate 80; iron oxide yellow; gelatin; titanium dioxide; macrogol 400; partially dehydrated liquid sorbitol - non-small cell lung cancer: velabine is indicated for the first line treatment of advanced non-small cell lung cancer, as a single agent or in combination. ,breast cancer: velabine is indicated for the treatment of advanced breast cancer after failure of standard therapy as a single agent or in combination.