Apo-Leflunomide New Zealand - English - Medsafe (Medicines Safety Authority)

apo-leflunomide

apotex nz ltd - leflunomide 20mg - tablet - 20 mg - active: leflunomide 20mg excipient: colloidal silicon dioxide crospovidone lactose magnesium stearate - apo-leflunomide is indicated for the treatment of: · rheumatoid arthritis, to improve signs and symptoms to retard joint destruction and to improve functional ability and quality of life. leflunomide may be used in patients who have failed to respond to other treatments or as a first line of treatment in patients who have a contraindication to other treatments. · active psoriatic arthritis. leflunomide is not indicated for the treatment of psoriasis that is not associated with manifestations of arthritic disease.

APO-LEFLUNOMIDE leflunomide 20mg tablet bottle Australia - English - Department of Health (Therapeutic Goods Administration)

apo-leflunomide leflunomide 20mg tablet bottle

arrotex pharmaceuticals pty ltd - leflunomide, quantity: 20 mg - tablet, film coated - excipient ingredients: magnesium stearate; crospovidone; maize starch; povidone; colloidal anhydrous silica; lactose monohydrate; microcrystalline cellulose; titanium dioxide; hypromellose; purified talc; iron oxide yellow; macrogol 6000 - treatment of active rheumatoid arthritis.,treatment of active psoriatic arthritis. leflunomide is not indicated for the treatment of psoriasis that is not associated with manifestations of arthritic disease. the combined use of leflunomide with other disease modifying antirheumatic drugs (dmards) has not been adequately studied (see precautions).

APO-LEFLUNOMIDE leflunomide 10mg tablet bottle Australia - English - Department of Health (Therapeutic Goods Administration)

apo-leflunomide leflunomide 10mg tablet bottle

arrotex pharmaceuticals pty ltd - leflunomide, quantity: 10 mg - tablet, film coated - excipient ingredients: microcrystalline cellulose; colloidal anhydrous silica; povidone; crospovidone; magnesium stearate; lactose monohydrate; maize starch; titanium dioxide; hypromellose; macrogol 4000 - treatment of active rheumatoid arthritis.,treatment of active psoriatic arthritis. leflunomide is not indicated for the treatment of psoriasis that is not associated with manifestations of arthritic disease. the combined use of leflunomide with other disease modifying antirheumatic drugs (dmards) has not been adequately studied (see precautions).

APO-LEFLUNOMIDE TABLET Canada - English - Health Canada

apo-leflunomide tablet

apotex inc - leflunomide - tablet - 20mg - leflunomide 20mg - disease-modifying antirheumatic agents

PMS-LEFLUNOMIDE TABLET Canada - English - Health Canada

pms-leflunomide tablet

pharmascience inc - leflunomide - tablet - 20mg - leflunomide 20mg - disease-modifying antirheumatic agents

PHL-LEFLUNOMIDE TABLET Canada - English - Health Canada

phl-leflunomide tablet

pharmel inc - leflunomide - tablet - 20mg - leflunomide 20mg - disease-modifying antirheumatic agents

DOM-LEFLUNOMIDE TABLET Canada - English - Health Canada

dom-leflunomide tablet

dominion pharmacal - leflunomide - tablet - 20mg - leflunomide 20mg - disease-modifying antirheumatic agents

MYLAN-LEFLUNOMIDE TABLET Canada - English - Health Canada

mylan-leflunomide tablet

mylan pharmaceuticals ulc - leflunomide - tablet - 20mg - leflunomide 20mg - disease-modifying antirheumatic agents

NU-LEFLUNOMIDE TABLET Canada - English - Health Canada

nu-leflunomide tablet

nu-pharm inc - leflunomide - tablet - 20mg - leflunomide 20mg - disease-modifying antirheumatic agents

NTP-LEFLUNOMIDE TABLET Canada - English - Health Canada

ntp-leflunomide tablet

teva canada limited - leflunomide - tablet - 20mg - leflunomide 20mg - disease-modifying antirheumatic agents