Bupropion Hydrochloride 150 mg
1 INDICATIONS AND USAGE Bupropion hydrochloride extended-release tablets (XL) are an aminoketone antidepressant, indicated for: • treatment of major de pressive disorder (MDD) ( 1.1 ) • prevention of seasonal affective disorder (SAD) ( 1.2 ) 1.1 Major Depressive Disorder (MDD) 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) ] . 1.2 Seasonal Affective Disorde (SAD) 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 (XL) in the prevention of seasonal major depressive episodes was established in 3 placebo-controlled trials in adult outpatients with a history of MDD with an autumn-winter seasonal pattern as defined in the DSM [see Clinical Studies (14.2) ].
slate run pharmaceuticals, llc
ROUND WHITE YH 102
YH 102 ROUND WHITE
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24 HR Bupropion Hydrochloride 150 MG Extended Release Oral Tablet
slate run pharmaceuticals, llc
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16 HOW SUPPLIED/STORAGE AND HANDLING
BUPROPION HYDROCHLORIDE Extended-Release Tablets USP (XL), 150 mg of
BUPROPION HYDROCHLORIDE, are white to pale yellow, round biconvex tablet with imprinting “YH 102” in bottles of 30 tablets (NDC 70436-010-04), 90 tablets (NDC 70436-010-06) and 500 tablets (NDC 70436-010-02).
BUPROPION HYDROCHLORIDE Extended-Release Tablets USP (XL), 300 mg of
BUPROPION HYDROCHLORIDE, are white to pale yellow, round biconvex tablet with imprinting “YH 101” in bottles of 30 tablets (NDC 70436-011-04), 90 tablets (NDC 70436-011-06) and 500 tablets (NDC 70436-011-02). Store at 20° to 25°C (68° to 77°F); excursions permitted to 15° to 30°C (59° to 86°F) [See USP Controlled Room Temperature]. Dispense in a tight, light-resistant container as defined in the USP with a child-resistant closure. Keep out of reach of children.
BUPROPION HYDROCHLORIDE Extended-Release Tablets USP (XL) may have an odor.
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