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Sertraline 100 MG Oral Tablet

INDICATIONS AND USAGE Major depressive Disorder Sertraline hydrochloride tablets are indicated for the treatment of Major depressive disorder in adults. The efficacy of sertraline in the treatment of a Major depressive episode was established in six to eight week controlled trials of adult outpatients whose diagnoses corresponded most closely to the DSM-III category of Major depressive disorder (see Clinical Trials under CLINICAL PHARMACOLOGY ). A Major depressive episode implies a prominent and relatively persistent depressed or dysphoric mood that usually interferes with daily functioning (nearly every day for at least 2 weeks); it should include at least 4 of the following 8 symptoms: change in appetite, change in sleep, psychomotor agitation or retardation, loss of interest in usual activities or decrease in sexual drive, increased fatigue, feelings of guilt or worthlessness, slowed thinking or impaired concentration, and a suicide attempt or suicidal ideation. The antidepressant action of sertraline in hospitalized depressed patients has not been adequately studied. The efficacy of sertraline in maintaining an antidepressant response for up to 44 weeks following 8 weeks of open-label acute treatment (52 weeks total) was demonstrated in a placebo-controlled trial. The usefulness of the drug in patients receiving sertraline for extended periods should be reevaluated periodically (see Clinical Trials under CLINICAL PHARMACOLOGY ). Premenstrual dysphoric Disorder (PMDD) Sertraline is indicated for the treament of Premenstrual dysphoric disorder (PMDD) in adults. The efficacy of sertraline in the treatment of PMDD was established in 2 placebo-controlled trials of female adult outpatients treated for 3 menstrual cycles who met criteria for the DSM-III-R/IV category of PMDD (see Clinical Trials under CLINICAL PHARMACOLOGY). The essential features of PMDD include markedly depressed mood, anxiety or tension, affective lability, and persistent anger or irritability. Other features include decreased interest in activities, difficulty concentrating, lack of energy, change in appetite or sleep, and feeling out of control. Physical symptoms associated with PMDD include breast tenderness, headache, joint and muscle pain, bloating and weight gain. These symptoms occur regularly during the luteal phase and remit within a few days following onset of menses; the disturbance markedly interferes with work or school or with usual social activities and relationships with others. In making the diagnosis, care should be taken to rule out other cyclical mood disorders that may be exacerbated by treatment with an antidepressant. The effectiveness of sertraline in long-term use, that is, for more than 3 menstrual cycles, has not been systematically evaluated in controlled trials. Therefore, the physician who elects to use sertraline for extended periods should periodically re-evaluate the long-term usefulness of the drug for the individual patient (see DOSAGE AND ADMINISTRATION).

Cobalt Laboratories Inc.


3 years ago OVAL WHITE SL 100 Sertraline 100 MG Oral Tablet

OVAL WHITE SL 100

3 years ago OVAL WHITE SL 100 Sertraline 100 MG Oral Tablet

SL 100 OVAL WHITE

HOW SUPPLIED Sertraline Hydrochloride Tablets capsular-shaped tablets, containing sertraline hydrochloride equivalent to 25, 50 and 100 mg of sertraline, are packaged in bottles. Sertraline Hydrochloride Tablets 25 mg: white to off-white film-coated, capsule-shaped, biconvex tablet with “SL†scoreline “25†on one side and “>†on the other side. NDC 16252-533-30 Bottles of 30 NDC 16252-533-90 Bottles of 90 NDC 16252-533-50 Bottles of 500 Sertraline Hydrochloride Tablets 50 mg: white to off-white film-coated, capsule-shaped, biconvex tablet with “SL†scoreline “50†on one side and “>†on the other side. NDC 16252-534-30 Bottles of 30 NDC 16252-534-90 Bottles of 90 NDC 16252-534-50 Bottles of 500 Sertraline Hydrochloride Tablets 100 mg: white to off-white, film-coated, capsule-shaped, biconvex tablet with “SL†scoreline “100†on one side and “>†on the other side. NDC 16252-535-30 Bottles of 30 NDC 16252-535-90 Bottles of 90 NDC 16252-535-50 Bottles of 500 Store at 25°C (77°F); excursions permitted to 15° - 30°C (59° - 86°F) [see USP Controlled Room Temperature]. Manufactured for: Cobalt Laboratories Bonita Springs, Florida U.S.A 34134 Item Number: 102-963-04 Date: March 2009


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