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The IFCN reviews fact-checkers for compliance with its code, and issues a certification to publishers who pass the audit. The certification lasts for one year, and fact-checkers must be re-examined annually to retain their certifications. [2] IFCN lists 170 organizations as members as of July 2024. [3]
Approved Drug Products with Therapeutic Equivalence Evaluations, commonly known as the Orange Book, is a publication produced by the United States Food and Drug Administration (FDA), as required by the Drug Price and Competition Act (Hatch-Waxman Act). The Hatch-Waxman Act was created to '"strike a balance between two competing policy interests ...
Usana Health Sciences, Inc., or USANA, is an American direct-selling company based in West Valley City, Utah. As of 2021, Usana was the 14th largest direct-selling company in the world by revenue. [3] The company manufactures most of its nutritional products, dietary supplements, and skincare products at a West Valley City facility. Its ...
Hydroxyzine, sold under the brand names Atarax and Vistaril among others, is an antihistamine medication. [ 8 ] It is used in the treatment of itchiness, anxiety, insomnia, and nausea (including that due to motion sickness). [ 8 ] It is used either by mouth or injection into a muscle. [ 8 ]
United States of America v. Regenerative Sciences, LLC, 741 F.3d 1314 (D.C. Cir. 2014), [1] was a decision in the United States Court of Appeals for the District of Columbia Circuit filed on February 4, 2014 concerning more than minimally manipulated cell therapies and whether they are considered part of medical practice or a drug, the latter subjecting it to regulation under the Food and Drug ...
Vilazodone was approved for medical use in the United States in 2011 [1] and in Canada in 2018. [8] In 2019, it was the 334th most commonly prescribed medication in the United States, with more than 900 thousand prescriptions. [9] The drug lost patent protection in June 2022 for adults and in July 2023 for pediatrics. [10]
Metandienone was formerly approved and marketed as a form of androgen replacement therapy for the treatment of hypogonadism in men, but has since been discontinued and withdrawn in most countries, including in the United States. [15][4][6] It was given at a dosage of 5 to 10 mg/day in men and 2.5 mg/day in women. [16][17][1] v. t.
Dutasteride was patented in 1993 by GlaxoSmithKline and was approved for medical use in 2001. [ 11 ] [ 7 ] In the United States and elsewhere, it is available as a generic medication . [ 4 ] In 2018, it was the 291st-most commonly prescribed medication in the US with more than 1 million prescriptions.
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