DIMETHYL FUMARATE SANDOZ dimethyl fumarate 240 mg modified release capsule blister pack Australië - Engels - Department of Health (Therapeutic Goods Administration)

dimethyl fumarate sandoz dimethyl fumarate 240 mg modified release capsule blister pack

sandoz pty ltd - dimethyl fumarate, quantity: 240 mg - capsule, modified release - excipient ingredients: colloidal anhydrous silica; glyceryl monostearate 40-55 per cent; gelatin; shellac; isopropyl alcohol; purified talc; propylene glycol; triethyl citrate; titanium dioxide; methacrylic acid - ethyl acrylate copolymer (1:1); croscarmellose sodium; butan-1-ol; methacrylic acid copolymer; iron oxide black; ethanol; sodium stearylfumarate; purified water; iron oxide yellow; brilliant blue fcf; polysorbate 80; strong ammonia solution - dimethyl fumarate sandoz is indicated in patients with relapsing multiple sclerosis to reduce the frequency of relapses and to delay the progression of disability.

DIBBS BROM-O-GAS 1000 FUMIGANT Australië - Engels - APVMA (Australian Pesticides and Veterinary Medicines Authority)

dibbs brom-o-gas 1000 fumigant

r a dibbs & sons pty ltd - methyl bromide - gas (soil fumigant) - methyl bromide gas active 1000.0 g/kg - mixed function pesticide - bed - plant - qps and cue treatment | buildings & similar structures qps & cue | cane products qps & approved cue | cereal grain - damping off - pythium ultimum | damping off - rhizoctonia spp. | damping off fungi | fusarium spp. | insect | nematode - soil borne plant parasitic | nutgrass | rodent, rat or mouse | stored product insect pests | weed seed | black rat/mouse | brown rat/mouse | fat hen | fusarium patch | fusarium spp. | mouse | prince of wales feather | pythium spp. | rat | rhizoctonia spp. | rodent | roof rat | soil fungi | victorian nutgrass | weed seeds | winter grass

METHYLPREDNISOLONE VIATRIS 1 G Israël - Engels - Ministry of Health

methylprednisolone viatris 1 g

genmedix , israel - methylprednisolone as hemisuccinate - lyophilized powder for solution for injection or infusion - methylprednisolone as hemisuccinate 1 g/vial - methylprednisolone - methylprednisolone - methylprednisolone mylan is indicated to treat any condition in which iv corticosteroid treatment is required such as: endocrine disorders, rheumatic disorders, collagen diseases, immune complex diseases, dermatologic diseases, allergic states, ophthalmic diseases, gastrointestinal diseases, respiratory diseases, hematologic disorders, management of neoplastic diseases, edematous states, nervous system disorders and organ transplantation.

METHYLPREDNISOLONE VIATRIS 500 MG Israël - Engels - Ministry of Health

methylprednisolone viatris 500 mg

genmedix , israel - methylprednisolone as hemisuccinate - lyophilized powder for solution for injection or infusion - methylprednisolone as hemisuccinate 500 mg/vial - methylprednisolone - methylprednisolone - methylprednisolone mylan is indicated to treat any condition in which iv corticosteroid treatment is required such as: endocrine disorders, rheumatic disorders, collagen diseases, immune complex diseases, dermatologic diseases, allergic states, ophthalmic diseases, gastrointestinal diseases, respiratory diseases, hematologic disorders, management of neoplastic diseases, edematous states, nervous system disorders and organ transplantation

METHYL BROMIDE Australië - Engels - APVMA (Australian Pesticides and Veterinary Medicines Authority)

methyl bromide

trical australia pty ltd - methyl bromide - unknown - methyl bromide gas active 0.0 - active constituent

METHYLPHENIDATE HYDROCHLORIDE tablet, extended release Verenigde Staten - Engels - NLM (National Library of Medicine)

methylphenidate hydrochloride tablet, extended release

lannett company, inc. - methylphenidate hydrochloride (unii: 4b3sc438hi) (methylphenidate - unii:207zz9qz49) - methylphenidate hydrochloride 18 mg - methylphenidate hcl extended-release tablets are indicated for the treatment of attention deficit hyperactivity disorder (adhd) in children 6 years of age and older, adolescents, and adults up to the age of 65 [see clinical studies (14)] . a diagnosis of attention deficit hyperactivity disorder (adhd; dsm-iv) implies the presence of hyperactive-impulsive or inattentive symptoms that caused impairment and were present before age 7 years. the symptoms must cause clinically significant impairment, e.g., in social, academic, or occupational functioning, and be present in two or more settings, e.g., school (or work) and at home. the symptoms must not be better accounted for by another mental disorder. for the inattentive type, at least six of the following symptoms must have persisted for at least 6 months: lack of attention to details/careless mistakes; lack of sustained attention; poor listener; failure to follow through on tasks; poor organization; avoids tasks requiring sustained mental effort; loses things; e

METHYLDOPA tablet, film coated Verenigde Staten - Engels - NLM (National Library of Medicine)

methyldopa tablet, film coated

accord healthcare inc. - methyldopa (unii: 56lh93261y) (methyldopa anhydrous - unii:m4r0h12f6m) - methyldopa anhydrous 125 mg - hypertension. methyldopa is contraindicated in patients: - with active hepatic disease, such as acute hepatitis and active cirrhosis. - with liver disorders previously associated with methyldopa therapy (see warnings ). - with hypersensitivity to any component of this product. - on therapy with monoamine oxidase (mao) inhibitors.

METHYLDOPA tablet Verenigde Staten - Engels - NLM (National Library of Medicine)

methyldopa tablet

mylan pharmaceuticals inc. - methyldopa (unii: 56lh93261y) (methyldopa anhydrous - unii:m4r0h12f6m) - methyldopa anhydrous 250 mg - hypertension. methyldopa is contraindicated in patients:

METHYLDOPA tablet Verenigde Staten - Engels - NLM (National Library of Medicine)

methyldopa tablet

mylan institutional inc. - methyldopa (unii: 56lh93261y) (methyldopa anhydrous - unii:m4r0h12f6m) - methyldopa anhydrous 500 mg - hypertension. methyldopa is contraindicated in patients: - with active hepatic disease, such as acute hepatitis and active cirrhosis. - with liver disorders previously associated with methyldopa therapy (see warnings). - with hypersensitivity to any component of this product. - on therapy with monoamine oxidase (mao) inhibitors.