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HSA Product

WELLBUTRIN SR TABLETS 150 mg

Product approved by Health Sciences Authority (SG)

Basic Information

WELLBUTRIN SR TABLETS 150 mg

TABLET, FILM COATED

Regulatory Information

SIN10983P

June 16, 1999

Prescription Only

Therapeutic

ORAL

August 10, 2023

June 3, 2025

XN06AX12

Company Information

GLAXOSMITHKLINE PTE LTD

GLAXOSMITHKLINE PTE LTD

Active Ingredients

BUPROPION HCl

Strength: 150 mg

Detailed Information

Contraindications

**Contraindications** _WELLBUTRIN SR_ is contraindicated in patients with hypersensitivity to bupropion or any of the other components of the preparation. _WELLBUTRIN SR_ is contraindicated in patients with a seizure disorder. _WELLBUTRIN SR_ is contraindicated in patients undergoing abrupt discontinuation of alcohol or sedatives. _WELLBUTRIN SR_ tablets contain bupropion and should not be administered to patients currently being treated with any other preparation containing bupropion as the incidence of seizures is dose dependent. _WELLBUTRIN SR_ is contraindicated in patients with a current or previous diagnosis of bulimia or anorexia nervosa as a higher incidence of seizures was seen in this patient population when an immediate release form of bupropion was administered. Concomitant use of _WELLBUTRIN SR_ and monoamine oxidase inhibitors (MAOIs) is contraindicated. At least 14 days should elapse between discontinuation of MAOIs and initiation of treatment with _WELLBUTRIN SR_ tablets.

Indication Information

**Indications** _WELLBUTRIN SR_ is indicated for the treatment of major depressive episodes.

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