What are the regulations regarding the distribution of pharmaceuticals?

In Nebraska, the distribution of pharmaceuticals is regulated by both the U.S. Food and Drug Administration (FDA) and the Nebraska Board of Pharmacy. Under FDA regulations, pharmaceuticals must be distributed only by licensed pharmacies that have been approved by the FDA. These pharmacies must have the appropriate licensing, training, and equipment needed to distribute pharmaceuticals safely and legally. Additionally, all transactions must be documented. The Nebraska Board of Pharmacy also regulates the distribution and sale of pharmaceuticals in the state. Pharmacists must be licensed by the Board and receive continuing education credits every two years to ensure they are up-to-date on the latest regulations and changes. Pharmacists are also responsible for properly labeling and storing the medications and tracking the distribution and sale of each drug. These regulations are put in place to ensure that all pharmaceuticals are distributed and sold safely and legally in Nebraska. This is important for ensuring that all medications are properly prescribed and used, and also that consumers do not become ill or suffer other adverse effects as a result of improper use.

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What are the regulations regarding the distribution of pharmaceuticals?

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