How does the law regulate the manufacture of counterfeit drugs?

In North Carolina, pharmaceutical law works to regulate the manufacture of counterfeit drugs. By law, pharmaceuticals must be manufactured according to strict standards in order to be legally sold in the state. These standards are meant to ensure the drugs are safe and effective for their intended uses. Counterfeit drugs are not produced under these pharmaceutical manufacturing standards. To protect consumers, North Carolina regulates their manufacture by requiring any company wishing to produce counterfeit drugs to be licensed by the state. This license is granted only after an inspection of the manufacturing facility and a review of the processes and materials used in the production of the drugs. In addition, North Carolina has criminalized the sale of counterfeit drugs. It is a Class H felony, punishable by up to eight months in prison and a $5,000 fine, to knowingly sell or transport counterfeit medication. If the counterfeited drugs result in an injury, it is a Class I felony with a potential four-year prison sentence and $10,000 fine. Finally, North Carolina requires that all drugs produced within the state be marked with an identifying number or symbol. This allows regulators to identify counterfeit products and trace them back to their source. By regulating the manufacture of counterfeit drugs, North Carolina is able to protect the safety of its citizens and ensure that all medication produced in the state meets the legal standards.

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How does the law regulate the manufacture of counterfeit drugs?

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