IMIPENEM-CILASTATIN RICHET 500MG/FCO. AMP. POLVO PARA SOLUCIÓN INYECTABLE I.V. POR INFUSIÓN. Panama - Inggris - Ministerio de Salud (Dirección Nacional de Farmacia Y Drogas)

imipenem-cilastatin richet 500mg/fco. amp. polvo para solución inyectable i.v. por infusión.

laboratorios richet, s.a. - imipenem anhidro (monohidrato) - imipenem anhidro (monohidrato)....500.00 mg / cilastatina Ácido (sal sÓdica)....500.00 mg

SODIUM VALPROATE AGUETTANT SOLUTION FOR INJECTION 400MG4ML Singapura - Inggris - HSA (Health Sciences Authority)

sodium valproate aguettant solution for injection 400mg4ml

aguettant asia pacific pte. ltd. - sodium valproate - injection, solution - sodium valproate 400mg/4ml

Lykaspetin 500 mg/500 mg Powder For Injection (I.V.) Filipina - Inggris - FDA (Food And Drug Administration)

lykaspetin 500 mg/500 mg powder for injection (i.v.)

ambica international corporation; distributor: ambica international corporation - imipenem (as monohydrate) , cilastatin (as sodium) - powder for injection (i.v.) - 500 mg/500 mg

Tenam 500 500 mg/500 mg Powder For Injection (Iv) Filipina - Inggris - FDA (Food And Drug Administration)

tenam 500 500 mg/500 mg powder for injection (iv)

jlt pharma, inc.; distributor: jlt pharma, inc. - imipenem (as monohydrate) , cilastatin (as sodium) - powder for injection (iv) - 500 mg/500 mg

Imaxin 500 mg/500 mg Powder for Injection (I.V.) Filipina - Inggris - FDA (Food And Drug Administration)

imaxin 500 mg/500 mg powder for injection (i.v.)

amb hk enterprises inc.; distributor: amb hk enterprises inc. - imipenem (as monohydrate) , cilastatin (as sodium) - powder for injection (i.v.) - 500 mg/500 mg

PZBACTAM 4 g/500 mg Powder For Iv Injection Filipina - Inggris - FDA (Food And Drug Administration)

pzbactam 4 g/500 mg powder for iv injection

eon pharmatek inc.; distributor: eon pharmatek inc. - piperacillin (as sodium) , tazobactam (as sodium) - powder for iv injection - 4 g/500 mg

DIVALPROEX SODIUM tablet, delayed release Amerika Serikat - Inggris - NLM (National Library of Medicine)

divalproex sodium tablet, delayed release

ncs healthcare of ky, inc dba vangard labs - divalproex sodium (unii: 644vl95ao6) (valproic acid - unii:614oi1z5wi) - valproic acid 250 mg - divalproex sodium is a valproate and is indicated for the treatment of the manic episodes associated with bipolar disorder. a manic episode is a distinct period of abnormally and persistently elevated, expansive, or irritable mood. typical symptoms of mania include pressure of speech, motor hyperactivity, reduced need for sleep, flight of ideas, grandiosity, poor judgment, aggressiveness, and possible hostility. the efficacy of divalproex sodium was established in 3 week trials with patients meeting dsm-iii-r criteria for bipolar disorder who were hospitalized for acute mania [see clinical studies (14.1)] . the safety and effectiveness of divalproex sodium for long-term use in mania, i.e., more than 3 weeks, has not been demonstrated in controlled clinical trials. therefore, healthcare providers who elect to use divalproex sodium for extended periods should continually reevaluate the long-term usefulness of the drug for the individual patient. divalproex sodium delayed-release tablets are indicated as monothe

DIVALPROEX SODIUM tablet, film coated, extended release Amerika Serikat - Inggris - NLM (National Library of Medicine)

divalproex sodium tablet, film coated, extended release

ncs healthcare of ky, inc dba vangard labs - divalproex sodium (unii: 644vl95ao6) (valproic acid - unii:614oi1z5wi) - valproic acid 250 mg - divalproex sodium extended-release tablets are a valproate and are indicated for the treatment of acute manic or mixed episodes associated with bipolar disorder, with or without psychotic features. a manic episode is a distinct period of abnormally and persistently elevated, expansive, or irritable mood. typical symptoms of mania include pressure of speech, motor hyperactivity, reduced need for sleep, flight of ideas, grandiosity, poor judgment, aggressiveness, and possible hostility. a mixed episode is characterized by the criteria for a manic episode in conjunction with those for a major depressive episode (depressed mood, loss of interest or pleasure in nearly all activities). the efficacy of divalproex sodium extended-release tablets is based in part on studies of divalproex sodium delayed-release tablets in this indication, and was confirmed in a 3-week trial with patients meeting dsm-iv tr criteria for bipolar i disorder, manic or mixed type, who were hospitalized for acute mania [see clinical studies (

DIVALPROEX SODIUM- divalproex sodium tablet, delayed release Amerika Serikat - Inggris - NLM (National Library of Medicine)

divalproex sodium- divalproex sodium tablet, delayed release

teva pharmaceuticals usa, inc. - divalproex sodium (unii: 644vl95ao6) (valproic acid - unii:614oi1z5wi) - valproic acid 125 mg - divalproex sodium delayed-release tablets are a valproate and are indicated for the treatment of the manic episodes associated with bipolar disorder. a manic episode is a distinct period of abnormally and persistently elevated, expansive, or irritable mood. typical symptoms of mania include pressure of speech, motor hyperactivity, reduced need for sleep, flight of ideas, grandiosity, poor judgment, aggressiveness, and possible hostility. the efficacy of divalproex sodium delayed-release tablets was established in 3 week trials with patients meeting dsm-iii-r criteria for bipolar disorder who were hospitalized for acute mania [see clinical studies (14.1)]. the safety and effectiveness of divalproex sodium delayed-release tablets for long-term use in mania, i.e., more than 3 weeks, has not been demonstrated in controlled clinical trials. therefore, healthcare providers who elect to use divalproex sodium delayed-release tablets for extended periods should continually reevaluate the long-term usefulness of the dr