Bupropion Hydrochloride

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Sun Pharma recalls 2.7 lakh bottles of antidepressant in US

Sun Pharma is recalling over 2.7 lakh bottles of bupropion hydrochloride extended-release tablets used for treatment of major depressive disorder in the US due to failed dissolution specifications.
Cadila's 20k bottles of anti-depressant recalled in US

Over 20,500 bottles of anti- depressant Bupropion Hydrochloride extended release tablets made by Cadila Healthcare are being recalled by Amerisource Health Services for failed dissolution specifications.
Sun Pharma recalls 31,762 bottles of antidepressant drug in US

The recall has been initiated by Sun Pharmaceutical Industries Inc for 31,762 bottles of bupropion hydrochloride extended-release tablets, USP (SR) in the strength of 150 mg, the US Food and Drug Administration (USFDA) said in its latest Enforcement Report.

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Bupropion Hydrochloride

Sun Pharma recalls 2.7 lakh bottles of antidepressant in US

Cadila's 20k bottles of anti-depressant recalled in US

Sun Pharma recalls 31,762 bottles of antidepressant drug in US