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NDC 16729-0443-16

BUPROPION HYDROCHLORIDE 150 mg/1 TABLET, EXTENDED RELEASE

Accord Healthcare Inc.

Available — 2-Day Shipping
NDC
16729-0443-16
Generic Name
BUPROPION HYDROCHLORIDE
Brand Name
BUPROPION HYDROCHLORIDE
Strength
150 mg/1
Dosage Form
TABLET, EXTENDED RELEASE
Route
ORAL
Package Size
—
Labeler
Accord Healthcare Inc.

FDA Drug Information

Indications & Usage

1 INDICATIONS AND USAGE 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 ) 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 formulat…

Source: FDA. For professional use only. Not a substitute for prescribing information.

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Other BUPROPION HYDROCHLORIDE NDC Codes

60505-0157-01100 mg/1TABLET, FILM COATED
2-Day
43547-0288-10100 mg/1TABLET, FILM COATED, EXTENDED RELEASE
2-Day
50228-0175-01150 mg/1TABLET, FILM COATED, EXTENDED RELEASE
2-Day
16729-0443-15150 mg/1TABLET, EXTENDED RELEASE
2-Day
16729-0443-10150 mg/1TABLET, EXTENDED RELEASE
2-Day

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