South Africa - English - South African Health Products Regulatory Authority (SAHPRA)

apotex sa (pty) ltd - tablet - see ingredients - each tablet contains atenolol 100,0 mg

South Africa - English - South African Health Products Regulatory Authority (SAHPRA)

apotex sa (pty) ltd - tablet - see ingredients - each tablet contains atenolol 50,0 mg

South Africa - English - South African Health Products Regulatory Authority (SAHPRA)

apotex sa (pty) ltd - capsules - see ingredients - each capsule contains nifedipine 5,0 mg

South Africa - English - South African Health Products Regulatory Authority (SAHPRA)

apotex sa (pty) ltd - tablet - see ingredients - each tablet contains clomipramine hydrochloride 50,0 mg

South Africa - English - South African Health Products Regulatory Authority (SAHPRA)

apotex sa (pty) ltd - tablet - see ingredients - each tablet contains alprazolam 0,25 mg

South Africa - English - South African Health Products Regulatory Authority (SAHPRA)

apotex sa (pty) ltd - tablet - see ingredients - each tablet contains flurbiprofen 50,0 mg

South Africa - English - South African Health Products Regulatory Authority (SAHPRA)

apotex sa (pty) ltd - tablet - see ingredients - each tablet contains allopurinol 100 mg

South Africa - English - South African Health Products Regulatory Authority (SAHPRA)

apotex sa (pty) ltd - tablet - see ingredients - each tablet contains flurbiprofen 100,0 mg

United States - English - NLM (National Library of Medicine)

apotex corp. - etodolac (unii: 2m36281008) (etodolac - unii:2m36281008) - etodolac 200 mg - carefully consider the potential benefits and risks of etodolac and other treatment options before deciding to use etodolac.  use the lowest effective dose for the shortest duration consistent with individual patient treatment goals (see warnings ). etodolac capsules are indicated: • for acute and long-term use in the management of signs and symptoms of the following: - osteoarthritis - rheumatoid arthritis • for the management of acute pain etodolac is contraindicated in patients with known hypersensitivity to etodolac or other ingredients in etodolac capsules. etodolac should not be given to patients who have experienced asthma, urticaria, or other allergic-type reactions after taking aspirin or other nsaids. severe, rarely fatal, anaphylactic-like reactions to nsaids have been reported in such patients (see warnings, anaphylactoid reactions and precautions , pre-existing asthma ). - in the setting of coronary artery bypass graft (cabg) surgery (see warnings )

United States - English - NLM (National Library of Medicine)

apotex corp. - etodolac (unii: 2m36281008) (etodolac - unii:2m36281008) - etodolac 400 mg - carefully consider the potential benefits and risks of etodolac and other treatment options before deciding to use etodolac. use the lowest effective dose for the shortest duration consistent with individual patient treatment goals (see warnings ). etodolac tablets, usp are indicated: - for acute and long-term use in the management of signs and symptoms of the following: osteoarthritis rheumatoid arthritis - osteoarthritis - rheumatoid arthritis - for the management of acute pain etodolac is contraindicated in patients with known hypersensitivity to etodolac. etodolac should not be given to patients who have experienced asthma, urticaria, or other allergic-type reactions after taking aspirin or other nsaids. severe, rarely fatal, anaphylactic-like reactions to nsaids have been reported in such patients (see warnings, anaphylactoid reactions and precautions, pre-existing asthma ). - etodolac tablets are contraindicated in the setting of coronary artery bypass graft (cabg) surgery (see warnings ).