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Although most recently in the news for their misuse by professional the thaiger pharma stanozolol tablets growing illegality into treatment for steroid abuseand use as a prescription medicine from 2006 to 2007 (Gonzalez-Gonzalez et al., 2008), these are likely to still be available in the American market since the FDA approved their manufacture and sale by a US company known as Gilead Sciences (Gilead) in October 2008 (Saketmari et al., 2009). A key question in considering whether a product has been "un-patentable" is whether such a product ever actually existed in the United States. As a reference, the FDA's "un-patentable" designation does not necessarily imply that the manufacturer is in the process of creating such a product but rather that the product was created during a period when none of the elements of the patent have been created. For example, if the US patent is extended for more than 3 years, the applicant is unlikely to come up with a product that would be patentable. In other words, even though a certain drug may have been developed at one time and subsequently patented by another company, the idea and process for developing it has never been patented, which does not render the drug itself "un-patentable." In the case of benzimidazoles, a US-based company, GlaxoSmithKline, is currently in the process of obtaining a US patent on an investigational new drug application for the use of bupropion on the treatment of bipolar disorder. While in late-stage development, bupropion may be more easily marketed in the United States, in the interim, all it has to show is its potential to decrease the burden of treatment-resistant bipolar disorder in bipolar patients, which is what the FDA expects it can do. To provide an idea of potential market size, there are between 300,000 and 400,000 people on the waiting list for early-stage clinical trials of bupropion or a related antidepressant agent (Kelliman, 2010a). As the FDA currently maintains that all current bupropion/selective serotonin reuptake inhibitor trials in bipolar disorder (B6) subjects "with a prior diagnosis" should be suspended "until there have been sufficient studies of bupropion in bipolar disorder in patients free of serious suicidal or self-harm behaviors or those with mild severe depression" (Gonzalez-Gonzalez vs. Gonzales-Gonzales et. al., 2012; see also Diamanti-Kandarakis et al., 2011), the waiting list for any new treatments for bipolar Related Article: