Budesonide Te Arai New Zealand - English - Medsafe (Medicines Safety Authority)

budesonide te arai

te arai biofarma limited - budesonide 3mg - modified release capsule - 3 mg - active: budesonide 3mg excipient: gelatin   ethylcellulose dispersion type b ink black 10a2 iron oxide black iron oxide red methacrylic acid copolymer polysorbate 80 purified talc sugar spheres titanium dioxide   triethyl citrate - indicated for the induction of remission in patients with mild to moderate crohn's disease affecting the ileum and/or the ascending colon.

BUDESONIDE INHALATION SUSPENSION suspension United States - English - NLM (National Library of Medicine)

budesonide inhalation suspension suspension

ritedose pharmaceuticals, llc - budesonide (unii: q3oks62q6x) (budesonide - unii:q3oks62q6x) - 1.1 maintenance treatment of asthma budesonide inhalation suspension is indicated for the maintenance treatment of asthma and as prophylactic therapy in children 12 months to 8 years of age. limitations of use: - budesonide inhalation suspension is not indicated for the relief of acute bronchospasm. the use of budesonide inhalation suspension is contraindicated in the following conditions: - primary treatment of status asthmaticus or other acute episodes of asthma where intensive measures are required. - hypersensitivity to budesonide or any of the ingredients of budesonide inhalation suspension [see warnings and precautions (5.3), description (11), adverse reactions (6.2)] . 8.1 pregnancy risk summary there are no adequate well-controlled studies of budesonide inhalation suspension in pregnant women. however, there are published studies on the use of budesonide, the active ingredient in budesonide inhalation suspension, in pregnant women. in animal reproduction studies, budesonide, administered by the su

Novolizer Budesonide 400 micrograms inhalation powder Ireland - English - HPRA (Health Products Regulatory Authority)

novolizer budesonide 400 micrograms inhalation powder

mylan ire healthcare limited - budesonide - powder for inhalation - 400 microgram(s) - glucocorticoids; budesonide

Novolizer® Budesonide 200 micrograms Inhalation Powder Ireland - English - HPRA (Health Products Regulatory Authority)

novolizer® budesonide 200 micrograms inhalation powder

mylan ire healthcare limited - budesonide - powder for inhalation - 200 microgram(s) - glucocorticoids; budesonide

BUDICORT TURBUHALER 200 MCGDOSE Israel - English - Ministry of Health

budicort turbuhaler 200 mcgdose

astrazeneca (israel) ltd - budesonide - powder for inhalation - budesonide 200 mcg/dose - budesonide - budesonide - bronchial asthma.

BUDICORT TURBUHALER 100 MCGDOSE Israel - English - Ministry of Health

budicort turbuhaler 100 mcgdose

astrazeneca (israel) ltd - budesonide - powder for inhalation - budesonide 100 mcg/dose - budesonide - budesonide - bronchial asthma.

BUDESON 3 MG CAPSULES Israel - English - Ministry of Health

budeson 3 mg capsules

rafa laboratories ltd - budesonide - capsules - budesonide 3 mg - budesonide - budesonide - acute mild to moderate crohn’s disease with involvement of the ileum (twisted intestine) and/or ascending colon (part of large bowel). collagenous colitis.autoimmune hepatitis.

MIFLONIDE POWDER FOR INHALATION 200 MCGCAPSULE Israel - English - Ministry of Health

miflonide powder for inhalation 200 mcgcapsule

novartis israel ltd - budesonide - capsules - budesonide 200 mcg - budesonide - budesonide - maintenance treatment of bronchial asthma.

MIFLONIDE POWDER FOR INHALATION 400 MCGCAPSULE Israel - English - Ministry of Health

miflonide powder for inhalation 400 mcgcapsule

novartis israel ltd - budesonide - capsules - budesonide 400 mcg - budesonide - budesonide - maintenance treatment of bronchial asthma.

CORTIMENT budesonide 9 mg prolonged  release tablet blister pack Australia - English - Department of Health (Therapeutic Goods Administration)

cortiment budesonide 9 mg prolonged release tablet blister pack

ferring pharmaceuticals pty ltd - budesonide, quantity: 9 mg - tablet, modified release - excipient ingredients: stearic acid; lecithin; microcrystalline cellulose; hyprolose; lactose monohydrate; silicon dioxide; magnesium stearate; methacrylic acid copolymer; purified talc; titanium dioxide; triethyl citrate - cortiment prolonged-release tablets are indicated in adults for induction of remission in patients with mild to moderate active ulcerative colitis (uc) where 5-asa treatment is not sufficient or not tolerated.