According to the FDA, a marketed generic version of the antidepressant buproprion hydrochloride XL (300 mg) is not equivalent to the brand name Wellbutrin XL and the product is being removed from the market. One year ago, another generic version of this drug was removed from the market for the same reason.
However, sometimes drug makers choose to remove drugs from the market even if there is no problem with their safety profile. In fact, from 2024
A drug recall occurs when a medication is removed from the market because the medication is deemed to be defective or possibly harmful. A market withdrawal
What is a drug recall? A drug manufacturer recalls a prescription or over-the-counter drug with the intent to remove it from the market. The
brand name Wellbutrin XL and the product is being removed from the market. One year ago, another generic version of this drug was removed from the market
Second, FDA has worked to remove unapproved drugs from the market. Many potentially unsafe drugs have been removed from the market since 2024, including several drugs with significant safety concerns.
A drug recall occurs when a medication is removed from the market because the medication is deemed to be defective or possibly harmful. A market withdrawal
A drug recall is when a medication is removed from the market because it is either defective or could be harmful.
manufacturer removes them from the market. Plans meeting certain requirements also can immediately remove brand name drugs from their formularies and
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