BuPROPion Hydrochloride 12 HR Bupropion Hydrochloride 150 MG Extended Release Oral Tablet
1 INDICATIONS AND USAGE 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 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 an aminoketone antidepressant, indicated for the treatment of major depressive disorder (MDD). ( 1 )
Watson Laboratories, Inc.
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16 HOW SUPPLIED/STORAGE AND HANDLING
BUPROPION HYDROCHLORIDE extended-release tablets USP (SR), 100 mg of
BUPROPION HYDROCHLORIDE, USP are white to off-white, round, unscored, bi-convex, film-coated tablets debossed with "WPI" over "858" on one side in bottles of 60 tablets (NDC 0591-3540-60) and 500 tablets (NDC 0591-3540-05).
BUPROPION HYDROCHLORIDE extended-release tablets USP (SR), 150 mg of
BUPROPION HYDROCHLORIDE, USP are white to off-white, round, unscored, bi-convex, film-coated tablets debossed with "WPI" over "839" on one side in bottles of 60 tablets (NDC 0591-3541-60), 250 tablets (NDC 0591-3541-25) and 500 tablets (NDC 0591-3541-05).
BUPROPION HYDROCHLORIDE extended-release tablets USP (SR), 200 mg of
BUPROPION HYDROCHLORIDE, USP are white to off-white, round, unscored, bi-convex, film-coated tablets debossed with "WPI" over "3385" on one side in bottles of 60 tablets (NDC 0591-3542-60). Store at 20° to 25°C (68° to 77°F) [See USP Controlled Room Temperature]. Protect from light and moisture.
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