Bupropion HCl ER XL

Strengths & Sizes

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NDC#31722-487-30
UPC Code331722487306
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NDC#31722-487-90
UPC Code331722487900
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NDC#31722-487-05
UPC Code331722487054
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NDC#31722-488-30
UPC Code331722488303
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NDC#31722-488-90
UPC Code331722488907
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NDC#31722-488-05
UPC Code331722488051
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Indications

Bupropion hydrochloride extended-release tablets (XL) are an aminoketone antidepressant, indicated for: treatment of major depressive disorder (MDD) (1.1); prevention of seasonal affective disorder (SAD) (1.2)

Product Info

Dosage FormTablet

TE CodeAB3

Brand ReferenceWellbutrin

Therapeutic CategoryNorepinephrine-Dopamine Reuptake Inhibitor (NDRI)

Pronunciationbyoo-PRO-pee-on

Inactive Ingredientsethyl cellulose, glyceryl behenate, hydrochloric acid, hypromellose, methacrylic acid and ethyl acrylate copolymer, microcrystalline cellulose, polyethylene glycol, povidone, silicon dioxide, sodium stearyl fumarate, titanium dioxide, triethyl citrate. In addition,150mg tablet contains FD&C blue #2 and 300 mg tablet contains iron oxide red, iron oxide yellow and talc. The tablets are printed with black ink which contains ammonium hydroxide, ferrosoferric oxide, propylene glycol and shellac. The insoluble shell of the extended-release tablet may remain intact during gastrointestinal transit and is eliminated in the feces.