APO-OLMESARTAN/AMLODIPINE/HCTZ 20/5/12.5 olmesartan medoxomil/amlodipine/hydrochlorothiazide 20/5/12.5 mg film-coated tablet blister pack 오스트레일리아 - 영어 - Department of Health (Therapeutic Goods Administration)

apo-olmesartan/amlodipine/hctz 20/5/12.5 olmesartan medoxomil/amlodipine/hydrochlorothiazide 20/5/12.5 mg film-coated tablet blister pack

arrotex pharmaceuticals pty ltd - hydrochlorothiazide, quantity: 12.5 mg; amlodipine besilate, quantity: 6.95 mg; olmesartan medoxomil, quantity: 20 mg - tablet, film coated - excipient ingredients: pregelatinised maize starch; silicified microcrystalline cellulose; isopropyl alcohol; magnesium stearate; lactose monohydrate; povidone; titanium dioxide; purified talc; iron oxide yellow; iron oxide red; polyvinyl alcohol; macrogol 3350; iron oxide black - apo-olmesartan/amlodipine/hctz 20/5/12.5 mg is indicated for the treatment of hypertension, either as replacement for olmesartan medoxomil, amlodipine and hydrochlorothiazide being already taken as separate tablets or as add-on therapy where a patient's blood pressure is not controlled on a dual combination. this fixed dose combination is not indicated for initial therapy.

APO-OLMESARTAN/AMLODIPINE/HCTZ 40/10/25 olmesartan medoxomil/amlodipine/hydrochlorothiazide 40/10/25 mg film-coated tablet blister pack 오스트레일리아 - 영어 - Department of Health (Therapeutic Goods Administration)

apo-olmesartan/amlodipine/hctz 40/10/25 olmesartan medoxomil/amlodipine/hydrochlorothiazide 40/10/25 mg film-coated tablet blister pack

arrotex pharmaceuticals pty ltd - amlodipine besilate, quantity: 13.9 mg; hydrochlorothiazide, quantity: 25 mg; olmesartan medoxomil, quantity: 40 mg - tablet, film coated - excipient ingredients: isopropyl alcohol; silicified microcrystalline cellulose; povidone; lactose monohydrate; pregelatinised maize starch; magnesium stearate; titanium dioxide; purified talc; iron oxide yellow; iron oxide red; polyvinyl alcohol; macrogol 3350 - apo-olmesartan/amlodipine/hctz 40/10/25 mg is indicated for the treatment of hypertension, either as replacement for olmesartan medoxomil, amlodipine and hydrochlorothiazide being already taken as separate tablets or as add-on therapy where a patient's blood pressure is not controlled on a dual combination. this fixed dose combination is not indicated for initial therapy.

APO-ROXITHROMYCIN roxithromycin 150 mg film coated tablets blister pack 오스트레일리아 - 영어 - Department of Health (Therapeutic Goods Administration)

apo-roxithromycin roxithromycin 150 mg film coated tablets blister pack

arrotex pharmaceuticals pty ltd - roxithromycin, quantity: 150 mg - tablet, film coated - excipient ingredients: colloidal anhydrous silica; glucose; sodium starch glycollate type b; hyprolose; povidone; hypromellose; titanium dioxide; propylene glycol; sodium starch glycollate type a; maize starch; purified talc; poloxamer; magnesium stearate - adults: roxithromycin is indicated for the treatment of the following types of mild to moderately severe infections caused by or likely to be caused by susceptible microorganisms: upper respiratory tract infection: acute pharyngitis, tonsillitis and sinusitis. lower respiratory tract infection: acute bronchitis and acute exacerbations of chronic bronchitis; community acquired pneumonia. skin and skin structure infections. nongonococcal urethritis. children: roxithromycin 150 mg tablets are indicated for the treatment of the following mild to moderately severe infections in children caused by or likely to be caused by susceptible microorganisms: acute pharyngitis. acute tonsillitis, impetigo. appropriate culture and sensitivity tests should be performed when necessary to determine organism susceptibility and thus treatment suitability. therapy with roxithromycin may be initiated before results of these tests are known; once results become available, appropriate therapy should be continued.

Linezolid 600mg, film coated Tablets 몰타 - 영어 - Malta Medicines Authority

linezolid 600mg, film coated tablets

central procurement & supplies unit ub002 industrial estate, san gwann sgn 3000, malta - linezolid - film-coated tablet - linezolid 600 mg - antibacterials for systemic use

Linezolid 600mg film-coated Tablets 몰타 - 영어 - Malta Medicines Authority

linezolid 600mg film-coated tablets

central procurement & supplies unit ub002 industrial estate, san gwann sgn 3000, malta - linezolid - film-coated tablet - linezolid 600 mg - antibacterials for systemic use

Linezolid 600mg film-coated Tablets 몰타 - 영어 - Malta Medicines Authority

linezolid 600mg film-coated tablets

central procurement & supplies unit ub002 industrial estate, san gwann sgn 3000, malta - linezolid - film-coated tablet - linezolid 600 mg - antibacterials for systemic use

Linezolid 600mg film-coated Tablets 몰타 - 영어 - Malta Medicines Authority

linezolid 600mg film-coated tablets

central procurement & supplies unit ub002 industrial estate, san gwann sgn 3000, malta - linezolid - film-coated tablet - linezolid 600 mg - antibacterials for systemic use

Linezolid 600 mg film-coated tablets 몰타 - 영어 - Malta Medicines Authority

linezolid 600 mg film-coated tablets

central procurement & supplies unit ub002 industrial estate, san gwann sgn 3000, malta - linezolid - film-coated tablet - linezolid 600 mg - antibacterials for systemic use

Linezolid Aurovitas 600 mg film-coated tablets 몰타 - 영어 - Malta Medicines Authority

linezolid aurovitas 600 mg film-coated tablets

central procurement & supplies unit ub002 industrial estate, san gwann sgn 3000, malta - linezolid - film-coated tablet - linezolid 600 mg - antibacterials for systemic use

LINEZOLID- linezolid tablet, film coated 미국 - 영어 - NLM (National Library of Medicine)

linezolid- linezolid tablet, film coated

glenmark pharmaceuticals inc., usa - linezolid (unii: isq9i6j12j) (linezolid - unii:isq9i6j12j) - linezolid 600 mg - linezolid tablets are indicated for the treatment of infections caused by susceptible strains of the designated microorganisms in the specific conditions listed below. linezolid tablets are not indicated for the treatment of gram-negative infections. it is critical that specific gram-negative therapy be initiated immediately if a concomitant gram-negative pathogen is documented or suspected [see warnings and precautions (5.4) ]. nosocomial pneumonia caused by staphylococcus aureus (methicillin-susceptible and -resistant isolates) or streptococcus pneumoniae [see clinical studies (14) ]. community-acquired pneumonia caused by streptococcus pneumoniae , including cases with concurrent bacteremia, or staphylococcus aureus (methicillin-susceptible isolates only) [see clinical studies (14) ]. complicated skin and skin structure infections, including diabetic foot infections, without concomitant osteomyelitis , caused by staphylococcus aureus (methicillin-susceptible and -resistant isolates), streptococcus py