PAINSTOP NIGHT-TIME PAIN RELIEVER oral liquid bottle Australia - engleză - Department of Health (Therapeutic Goods Administration)

painstop night-time pain reliever oral liquid bottle

care pharmaceuticals pty ltd - codeine phosphate hemihydrate, quantity: 1 mg/ml; paracetamol, quantity: 24 mg/ml; promethazine hydrochloride, quantity: 1.3 mg/ml - oral liquid, solution - excipient ingredients: purified water; sodium metabisulfite; sorbitol solution (70 per cent) (non-crystallising); propylene glycol; sucrose; disodium edetate; saccharin sodium; brilliant blue fcf; amaranth; phosphoric acid; ethanol; flavour - for the temporary relief of acute moderate pain when paracetamol alone is not sufficient and sedation is considered beneficial in patients over the age of 12 years ( see also contraindications and paediatric use)

4FARMERS 1080 liquid 30g/L Australia - engleză - APVMA (Australian Pesticides and Veterinary Medicines Authority)

4farmers 1080 liquid 30g/l

4 farmers australia pty ltd - sodium fluoroacetate - liquid concentrate - sodium fluoroacetate mineral-fluorine active 30.0 g/l - vertebrate poison

MOXXI POUR-ON FOR CATTLE AND RED DEER Australia - engleză - APVMA (Australian Pesticides and Veterinary Medicines Authority)

moxxi pour-on for cattle and red deer

abbey laboratories pty ltd - moxidectin; liquid hydrocarbon - topical solution/suspension - moxidectin anthelmintic active 5.0 g/l; liquid hydrocarbon solvent other 150.0 g/l - parasiticides

ROTARIX human rotavirus (live attenuated oral vaccine) oral liquid tube Australia - engleză - Department of Health (Therapeutic Goods Administration)

rotarix human rotavirus (live attenuated oral vaccine) oral liquid tube

glaxosmithkline australia pty ltd - rotavirus, quantity: 1000000 ccid50/dose - oral liquid, suspension - excipient ingredients: sucrose; water for injections; adipic acid; sodium hydroxide; glucose monohydrate; sodium chloride; potassium chloride; magnesium sulfate heptahydrate; ferric nitrate nonahydrate; dibasic sodium phosphate dihydrate; sodium pyruvate; folic acid; calcium pantothenate; inositol; choline chloride; nicotinamide; pyridoxine hydrochloride; thiamine hydrochloride; riboflavine; cystine; tyrosine; arginine; glycine; histidine; isoleucine; leucine; lysine; methionine; phenylalanine; threonine; tryptophan; serine; valine; glutamine; calcium chloride dihydrate; sodium bicarbonate - rotarix is indicated for the prevention of rotavirus gastroenteritis (see clinical trials).

ROTARIX human rotavirus (live attenuated oral vaccine) oral liquid tube (multi-monodose) Australia - engleză - Department of Health (Therapeutic Goods Administration)

rotarix human rotavirus (live attenuated oral vaccine) oral liquid tube (multi-monodose)

glaxosmithkline australia pty ltd - rotavirus, quantity: 1000000 ccid50/dose - oral liquid, suspension - excipient ingredients: sucrose; water for injections; adipic acid; sodium hydroxide; glucose monohydrate; sodium chloride; potassium chloride; magnesium sulfate heptahydrate; ferric nitrate nonahydrate; dibasic sodium phosphate dihydrate; sodium pyruvate; folic acid; calcium pantothenate; inositol; choline chloride; nicotinamide; pyridoxine hydrochloride; thiamine hydrochloride; riboflavine; cystine; tyrosine; arginine; glycine; histidine; isoleucine; leucine; lysine; methionine; phenylalanine; threonine; tryptophan; serine; valine; glutamine; calcium chloride dihydrate; sodium bicarbonate - rotarix is indicated for the prevention of rotavirus gastroenteritis (see clinical trials).

Pregabalin-AFT Pregabalin 20 mg/mL oral liquid solution bottle Australia - engleză - Department of Health (Therapeutic Goods Administration)

pregabalin-aft pregabalin 20 mg/ml oral liquid solution bottle

aft pharmaceuticals pty ltd - pregabalin, quantity: 20 mg/ml - oral liquid, solution - excipient ingredients: sucralose; monobasic sodium phosphate monohydrate; purified water; methyl hydroxybenzoate; dibasic sodium phosphate; flavour - pregabalin-aft is indicated for the treatment of neuropathic pain in adults.,pregabalin-aft is indicated as adjunctive therapy in adults with partial seizures with or without secondary generalisation.

CECLOR cefaclor 125mg/5mL (as monohydrate) powder for oral liquid Australia - engleză - Department of Health (Therapeutic Goods Administration)

ceclor cefaclor 125mg/5ml (as monohydrate) powder for oral liquid

viatris pty ltd - cefaclor monohydrate, quantity: 26.22 mg/ml (equivalent: cefaclor, qty 25 mg/ml) - oral liquid, powder for - excipient ingredients: methylcellulose; sodium lauryl sulfate; dimeticone 350; xanthan gum; erythrosine; sucrose; pregelatinised starch; flavour - ceclor is indicated for the treatment of the following types of infections caused by or likely to be caused by susceptible organisms: lower respiratory infections, including pneumonia, bronchitis and exacerbations of chronic bronchitis. upper respiratory tract infections, including pharyngitis, tonsillitis and otitis media. skin and skin structure infections. urinary tract infections including pyelonephritis and cystitis. note: 1. penicillin is the usual drug of choice in the treatment and prevention of streptococcal infections, including the prophylaxis of rheumatic fever. ceclor appears to be as effective as phenoxymethyl penicillin in the eradication of streptococci from the nasopharynx; however, substantial data establishing the efficacy of ceclor in the subsequent prevention of rheumatic fever are not available at present. 2. appropriate culture and susceptibility studies should be performed to determine susceptibility of the causative organism to cefaclor.

CECLOR cefaclor 250mg/5mL (as monohydrate) powder for oral liquid bottle Australia - engleză - Department of Health (Therapeutic Goods Administration)

ceclor cefaclor 250mg/5ml (as monohydrate) powder for oral liquid bottle

viatris pty ltd - cefaclor monohydrate, quantity: 52.45 mg/ml (equivalent: cefaclor, qty 50 mg/ml) - oral liquid, powder for - excipient ingredients: methylcellulose; sodium lauryl sulfate; dimeticone 350; xanthan gum; erythrosine; sucrose; pregelatinised starch; flavour - ceclor is indicated for the treatment of the following types of infections caused by or likely to be caused by susceptible organisms: lower respiratory infections, including pneumonia, bronchitis and exacerbations of chronic bronchitis. upper respiratory tract infections, including pharyngitis, tonsillitis and otitis media. skin and skin structure infections. urinary tract infections including pyelonephritis and cystitis. note: 1. penicillin is the usual drug of choice in the treatment and prevention of streptococcal infections, including the prophylaxis of rheumatic fever. ceclor appears to be as effective as phenoxymethyl penicillin in the eradication of streptococci from the nasopharynx; however, substantial data establishing the efficacy of ceclor in the subsequent prevention of rheumatic fever are not available at present. 2. appropriate culture and susceptibility studies should be performed to determine susceptibility of the causative organism to cefaclor.

NUELIN LIQUID Africa de Sud - engleză - South African Health Products Regulatory Authority (SAHPRA)

nuelin liquid

inova pharmaceuticals (pty) ltd - liquid - see ingredients - each 5,0 ml liquid contains theophylline 25,0 mg

Amitriptyline hydrochloride 10mg/5ml Oral solution Regatul Unit - engleză - myHealthbox

amitriptyline hydrochloride 10mg/5ml oral solution

wockhardt uk ltd - amitriptyline hydrochloride - oral solution - 10 mg/5ml - it is indicated for the treatment of: symptoms of depression (especially where sedation is required); nocturnal enuresis where organic pathology is excluded.