Bupropion hydrochloride
Bupropion hydrochloride is one of 8,063 medications in the MedPlain dataset. Key details — Brand name: Bupropion hydrochloride; Generic name: BUPROPION HYDROCHLORIDE; Manufacturer: Sun Pharmaceutical Industries, Inc..
| Brand name | Bupropion hydrochloride |
|---|---|
| Generic name | BUPROPION HYDROCHLORIDE |
| Manufacturer | Sun Pharmaceutical Industries, Inc. |
| Used for | 1 INDICATIONS AND USAGE Bupropion hydrochloride extended-release tablets, USP (XL) are 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, USP (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 o |
| Dosage | 2 DOSAGE AND ADMINISTRATION General: Increase dose gradually to reduce seizure risk. (2.1, 5.3) Periodically reassess the dose and need for maintenance treatment. (2.2) Major Depressive Disorder Starting dose: 150 mg once daily. Usual target dose: 300 mg once daily (2.2) After 4 days, may increase the dose to 300 mg once daily. (2.2) Seasonal Affective Disorder Initiate treatment in the autumn prior to onset of seasonal depressive symptoms. (2.3) Starting dose: 150 mg once daily. Usual target do |
| Warnings | WARNING: SUICIDAL THOUGHTS AND BEHAVIORS SUICIDALITY AND ANTIDEPRESSANT DRUGS Antidepressants increased the risk of suicidal thoughts and behavior in children, adolescents, and young adults in short-term trials. These trials did not show an increase in the risk of suicidal thoughts and behavior with antidepressant use in subjects aged 65 and older [see Warnings and Precautions (5.1)] . In patients of all ages who are started on antidepressant therapy, monitor closely for worsening, and for emerg |
| Active ingredient(s) | BUPROPION HYDROCHLORIDE |
| Route | ORAL |
| Official label | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=195b9970-0bc6-4f48-9450-a91292ad4618 |