Fintepla European Union - English - EMA (European Medicines Agency)

fintepla

ucb pharma s.a.   - fenfluramine hydrochloride - epilepsies, myoclonic - antiepileptics, - treatment of seizures associated with dravet syndrome as an add-on therapy to other antiepileptic medicines for patients 2 years of age and older.fintepla is indicated for the treatment of seizures associated with dravet syndrome and lennox-gastaut syndrome as an add-on therapy to other anti-epileptic medicines for patients 2 years of age and older.

FINTEPLA Israel - English - Ministry of Health

fintepla

medison pharma ltd - fenfluramine as hydrochloride - oral solution - fenfluramine as hydrochloride 2.2 mg / 1 ml - fenfluramine - fintepla is indicated for the treatment of seizures associated with dravet syndrome and lennox-gastaut syndrome as an add-on therapy to other anti-epileptic medicines for patients 2 years of age and older

Ponderax New Zealand - English - Medsafe (Medicines Safety Authority)

ponderax

seqirus (nz) ltd - fenfluramine hydrochloride 20mg - tablet - 20 mg - active: fenfluramine hydrochloride 20mg

Ponderax New Zealand - English - Medsafe (Medicines Safety Authority)

ponderax

seqirus (nz) ltd - fenfluramine hydrochloride 40mg - tablet - 40 mg - active: fenfluramine hydrochloride 40mg

Ponderax Pacaps New Zealand - English - Medsafe (Medicines Safety Authority)

ponderax pacaps

servier laboratories nz ltd - fenfluramine hydrochloride 60mg - modified release capsule - 60 mg - active: fenfluramine hydrochloride 60mg

PHENTERMINE JUNO ER phentermine (as hydrochloride) 40 mg extended release tablet blister pack Australia - English - Department of Health (Therapeutic Goods Administration)

phentermine juno er phentermine (as hydrochloride) 40 mg extended release tablet blister pack

juno pc holdings pty limited - phentermine hydrochloride, quantity: 49.7 mg - tablet, modified release - excipient ingredients: cetostearyl alcohol; sorbitol; maltodextrin; stearic acid; magnesium stearate; titanium dioxide; sunset yellow fcf aluminium lake; purified talc; polyvinyl alcohol; macrogol 3350; brilliant scarlet 4r aluminium lake - phentermine is an anorectic agent indicated in the management of obesity as a short-term adjunct in a medically monitored comprehensive regimen of weight reduction based, for example, on exercise, diet (caloric/kilojoule restriction) and behaviour modification in obese patients with a body mass index (bmi) of 30 kg/m2 or greater.,the treatment with phentermine can be initiated in overweight patients with a lower bmi (25 to 29.9 kg/m2), which increases the risk of morbidity from a number of disorders. secondary organic causes of obesity should be excluded by diagnosis before prescribing this agent.

PHENTERMINE JUNO ER phentermine (as hydrochloride) 30 mg extended release tablet blister pack Australia - English - Department of Health (Therapeutic Goods Administration)

phentermine juno er phentermine (as hydrochloride) 30 mg extended release tablet blister pack

juno pc holdings pty limited - phentermine hydrochloride, quantity: 37.275 mg - tablet, modified release - excipient ingredients: cetostearyl alcohol; sorbitol; maltodextrin; stearic acid; magnesium stearate; titanium dioxide; purified talc; iron oxide red; polyvinyl alcohol; macrogol 3350; ferrosoferric oxide - phentermine is an anorectic agent indicated in the management of obesity as a short-term adjunct in a medically monitored comprehensive regimen of weight reduction based, for example, on exercise, diet (caloric/kilojoule restriction) and behaviour modification in obese patients with a body mass index (bmi) of 30 kg/m2 or greater.,the treatment with phentermine can be initiated in overweight patients with a lower bmi (25 to 29.9 kg/m2), which increases the risk of morbidity from a number of disorders. secondary organic causes of obesity should be excluded by diagnosis before prescribing this agent.

PHENTERMINE JUNO ER phentermine (as hydrochloride) 15 mg extended release tablet blister pack Australia - English - Department of Health (Therapeutic Goods Administration)

phentermine juno er phentermine (as hydrochloride) 15 mg extended release tablet blister pack

juno pc holdings pty limited - phentermine hydrochloride, quantity: 18.6375 mg - tablet, modified release - excipient ingredients: cetostearyl alcohol; sorbitol; maltodextrin; stearic acid; magnesium stearate; titanium dioxide; sunset yellow fcf aluminium lake; purified talc; iron oxide yellow; brilliant blue fcf aluminium lake; polyvinyl alcohol; macrogol 3350 - phentermine is an anorectic agent indicated in the management of obesity as a short-term adjunct in a medically monitored comprehensive regimen of weight reduction based, for example, on exercise, diet (caloric/kilojoule restriction) and behaviour modification in obese patients with a body mass index (bmi) of 30 kg/m2 or greater.,the treatment with phentermine can be initiated in overweight patients with a lower bmi (25 to 29.9 kg/m2), which increases the risk of morbidity from a number of disorders. secondary organic causes of obesity should be excluded by diagnosis before prescribing this agent.

PHENTODUR phentermine (as hydrochloride) 40 mg modified release capsule blister pack Australia - English - Department of Health (Therapeutic Goods Administration)

phentodur phentermine (as hydrochloride) 40 mg modified release capsule blister pack

arrotex pharmaceuticals pty ltd - phentermine hydrochloride, quantity: 49.776 mg - capsule, modified release - excipient ingredients: liquid paraffin; lactose monohydrate; magnesium stearate; iron oxide black; sodium polystyrene sulfonate; sunset yellow fcf; titanium dioxide; gelatin; erythrosine; propylene glycol; ethanol; butan-1-ol; isopropyl alcohol; purified water; shellac; strong ammonia solution; potassium hydroxide - phentermine is an anorectic agent indicated in the management of obesity as a short-term adjunct in a medically monitored comprehensive regimen of weight reduction based, for example, on exercise, diet (caloric/kilojoule restriction) and behaviour modification in obese patients with a body mass index (bmi) of 30 kg/m2 or greater. the treatment with phentermine can be initiated in overweight patients with a lower bmi (25 to 29.9 kg/m2), which increases the risk of morbidity from a number of disorders. secondary organic causes of obesity should be excluded by diagnosis before prescribing this agent.

PHENTODUR phentermine (as hydrochloride) 30 mg modified release capsule blister pack Australia - English - Department of Health (Therapeutic Goods Administration)

phentodur phentermine (as hydrochloride) 30 mg modified release capsule blister pack

arrotex pharmaceuticals pty ltd - phentermine hydrochloride, quantity: 37.332 mg - capsule, modified release - excipient ingredients: gelatin; liquid paraffin; magnesium stearate; titanium dioxide; sodium polystyrene sulfonate; iron oxide red; lactose monohydrate; iron oxide black; propylene glycol; ethanol; butan-1-ol; isopropyl alcohol; purified water; shellac; strong ammonia solution; potassium hydroxide - phentermine is an anorectic agent indicated in the management of obesity as a short-term adjunct in a medically monitored comprehensive regimen of weight reduction based, for example, on exercise, diet (caloric/kilojoule restriction) and behaviour modification in obese patients with a body mass index (bmi) of 30 kg/m2 or greater. the treatment with phentermine can be initiated in overweight patients with a lower bmi (25 to 29.9 kg/m2), which increases the risk of morbidity from a number of disorders. secondary organic causes of obesity should be excluded by diagnosis before prescribing this agent.