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Recalls & Warnings October 02, 2008 FDA Permits Incorrect Labeling on Generic Wellbutrin XL, But May Require Drug to be Tested The FDA has acknowledged inconsistencies in the labeling of Budeprion XL, a generic version of the antidepressant Wellbutrin XL, according to an October 2, 2008 article from Dow Jones News service

It is classified as a research chemical, intended only for laboratory research and not for human use

2021, pp

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2025 Jun 19;18(6):928

Their established analytical profiles and continued presence within scientific literature have contributed to ongoing interest across multiple fields of peptide research