BUPROPION HYDROCHLORIDE- bupropion hydrochloride tablet, film coated, extended release Verenigde Staten - Engels - NLM (National Library of Medicine)

bupropion hydrochloride- bupropion hydrochloride tablet, film coated, extended release

mylan institutional inc. - bupropion hydrochloride (unii: zg7e5poy8o) (bupropion - unii:01zg3tpx31) - bupropion hydrochloride 100 mg - bupropion hydrochloride extended-release tablets (sr) are indicated for the treatment of major depressive disorder (mdd), as defined by the diagnostic and statistical manual (dsm ) . the efficacy of bupropion in the treatment of a major depressive episode was established in two 4-week controlled inpatient trials and one 6-week controlled outpatient trial of adult subjects with mdd [see clinical studies (14)] . the efficacy of bupropion hydrochloride extended-release tablets (sr) in maintaining an antidepressant response for up to 44 weeks following 8 weeks of acute treatment was demonstrated in a placebo-controlled trial [see clinical studies (14)] . - bupropion hydrochloride extended-release tablets (sr) are contraindicated in patients with a seizure disorder. - bupropion hydrochloride extended-release tablets (sr) are contraindicated in patients with a current or prior diagnosis of bulimia or anorexia nervosa as a higher incidence of seizures was observed in such patients treated with the immediate-releas

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

bupropion hydrochloride tablet, film coated

mylan institutional inc. - bupropion hydrochloride (unii: zg7e5poy8o) (bupropion - unii:01zg3tpx31) - bupropion hydrochloride 75 mg - bupropion hydrochloride tablets are indicated for the treatment of major depressive disorder (mdd), as defined by the diagnostic and statistical manual (dsm). the efficacy of bupropion hydrochloride tablets in the treatment of a major depressive episode was established in two 4-week controlled inpatient trials and one 6-week controlled outpatient trial of adult subjects with mdd [see clinical studies (14)] . - bupropion hydrochloride tablets are contraindicated in patients with a seizure disorder. - bupropion hydrochloride tablets are contraindicated in patients with a current or prior diagnosis of bulimia or anorexia nervosa as a higher incidence of seizures was observed in such patients treated with bupropion hydrochloride tablets [see warnings and precautions (5.3)]

BUPROPION HYDROCHLORIDE- bupropion hydrochloride tablet, film coated, extended release Verenigde Staten - Engels - NLM (National Library of Medicine)

bupropion hydrochloride- bupropion hydrochloride tablet, film coated, extended release

mylan institutional inc. - bupropion hydrochloride (unii: zg7e5poy8o) (bupropion - unii:01zg3tpx31) - bupropion hydrochloride extended-release tablets (xl) are indicated for the treatment of major depressive disorder (mdd), as defined by the diagnostic and statistical manual (dsm). the efficacy of the immediate-release formulation of bupropion was established in two 4-week controlled inpatient trials and one 6-week controlled outpatient trial of adult patients with mdd. the efficacy of the sustained-release formulation of bupropion in the maintenance treatment of mdd was established in a long-term (up to 44 weeks), placebo-controlled trial in patients who had responded to bupropion in an 8-week study of acute treatment [see clinical studies (14.1)] . bupropion hydrochloride extended-release tablets (xl) are indicated for the prevention of seasonal major depressive episodes in patients with a diagnosis of seasonal affective disorder (sad). the efficacy of bupropion hydrochloride extended-release tablets in the prevention of seasonal major depressive episodes was established in 3 placebo-controlled trials in a

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

salsalate tablet

method pharmaceuticals, llc - salsalate (unii: v9mo595c9i) (salsalate - unii:v9mo595c9i) - salsalate 500 mg

XYLOCAINE MPF- lidocaine hydrochloride injection, solution
XYLOCAINE- lidocaine hydrochloride injection, solution
XYLOCAINE MP Verenigde Staten - Engels - NLM (National Library of Medicine)

xylocaine mpf- lidocaine hydrochloride injection, solution xylocaine- lidocaine hydrochloride injection, solution xylocaine mp

fresenius kabi usa, llc - lidocaine hydrochloride anhydrous (unii: ec2cnf7xfp) (lidocaine - unii:98pi200987) - lidocaine hydrochloride anhydrous 10 mg in 1 ml - xylocaine (lidocaine hcl) injections are indicated for production of local or regional anesthesia by infiltration techniques such as percutaneous injection and intravenous regional anesthesia by peripheral nerve block techniques such as brachial plexus and intercostal and by central neural techniques such as lumbar and caudal epidural blocks, when the accepted procedures for these techniques as described in standard textbooks are observed. lidocaine hcl is contraindicated in patients with a known history of hypersensitivity to local anesthetics of the amide type.

CHLOROPROCAINE HYDROCHLORIDE injection, solution Verenigde Staten - Engels - NLM (National Library of Medicine)

chloroprocaine hydrochloride injection, solution

hikma pharmaceuticals usa inc. - chloroprocaine hydrochloride (unii: lt7z1yw11h) (chloroprocaine - unii:5yvb0pot2h) - chloroprocaine hydrochloride 20 mg in 1 ml - chloroprocaine hydrochloride injection 2% and 3%, in single dose vials, without methylparaben preservative, without edta, is indicated for the production of local anesthesia by infiltration, peripheral and central nerve block, including lumbar and caudal epidural blocks. chloroprocaine hydrochloride injection is not to be used for subarachnoid administration. chloroprocaine hydrochloride is contraindicated in patients hypersensitive (allergic) to drugs of the paba ester group. lumbar and caudal epidural anesthesia should be used with extreme caution in persons with the following conditions: existing neurological disease, spinal deformities, septicemia, and severe hypertension.

LIDOCAINE- lidocaine hydrochloride injection, solution
LIDOCAINE- lidocaine hydrochloride injection, solution Verenigde Staten - Engels - NLM (National Library of Medicine)

lidocaine- lidocaine hydrochloride injection, solution lidocaine- lidocaine hydrochloride injection, solution

hikma pharmaceuticals usa inc. - lidocaine hydrochloride (unii: v13007z41a) (lidocaine - unii:98pi200987) - lidocaine hydrochloride 10 mg in 1 ml - lidocaine hcl injections are indicated for production of local anesthesia by infiltration techniques such as percutaneous injection and by peripheral nerve block techniques such as brachial plexus and intercostal, when the accepted procedures for these techniques as described in standard textbooks are observed. lidocaine hcl is contraindicated in patients with a known history of hypersensitivity to local anesthetics of the amide type.

LIDOCAINE HYDROCHLORIDE injection, solution
LIDOCAINE HYDROCHLORIDE injection, solution Verenigde Staten - Engels - NLM (National Library of Medicine)

lidocaine hydrochloride injection, solution lidocaine hydrochloride injection, solution

hikma pharmaceuticals usa inc. - lidocaine hydrochloride (unii: v13007z41a) (lidocaine - unii:98pi200987) - lidocaine hydrochloride anhydrous 10 mg in 1 ml - lidocaine hcl injections are indicated for production of local or regional anesthesia by infiltration techniques such as percutaneous injection and by peripheral nerve block techniques such as brachial plexus and intercostal and by central neural techniques such as lumbar and caudal epidural blocks, when the accepted procedures for these techniques as described in standard textbooks are observed.  lidocaine hcl is contraindicated in patients with a known history of hypersensitivity to local anesthetics of the amide type.

EAR CLEANSING- alcohol, lactic acid, benzoic acid, and salicylic acid liquid Verenigde Staten - Engels - NLM (National Library of Medicine)

ear cleansing- alcohol, lactic acid, benzoic acid, and salicylic acid liquid

tomlyn products, a division of vetoquinol usa, inc. - alcohol (unii: 3k9958v90m) (alcohol - unii:3k9958v90m), lactic acid, unspecified form (unii: 33x04xa5at) (lactic acid, unspecified form - unii:33x04xa5at), benzoic acid (unii: 8skn0b0mim) (benzoic acid - unii:8skn0b0mim), salicylic acid (unii: o414pz4lpz) (salicylic acid - unii:o414pz4lpz) - alcohol 11.08 ml in 1 ml - tomlyn's veterinarian formulated ear cleaner is specially formulated to deodorize and gently clean, dry and acidify the external ear canal. this provides an environment which promotes maintenance of healthy ears, and aids in the prevention of external ear infections.

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

repaglinide tablet

mylan institutional inc. - repaglinide (unii: 668z8c33lu) (repaglinide - unii:668z8c33lu) - repaglinide 0.5 mg