Search Results for keywords:"DEA notice"

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Search Results: keywords:"DEA notice"

  • Type:Notice
    Citation:90 FR 13882
    Reading Time:about 7 minutes

    The Drug Enforcement Administration (DEA) has decided to revoke Joely Keen's DEA registration because she is no longer authorized to handle controlled substances in Texas. Her licenses to practice as an advanced practice registered nurse (APRN) and registered nurse in Texas have been revoked, and she lacks a necessary prescriptive authority agreement with a supervising physician. Without these, she cannot legally prescribe or dispense controlled substances, resulting in the loss of her DEA registration. The order becomes effective on April 28, 2025.

    Simple Explanation

    Joely Keen lost her special permission to give out certain medicines because she's no longer allowed to do that in Texas, and her special nurse licenses were taken away. This means she can't write prescriptions, and another special rule will make her permission officially gone on April 28, 2025.

  • Type:Notice
    Citation:86 FR 8381
    Reading Time:about a minute or two

    Noramco Inc has applied to the Drug Enforcement Administration (DEA) to become a bulk manufacturer of certain controlled substances, including synthetic versions of Marihuana Extract, Marihuana, and Tetrahydrocannabinols. The company intends to produce these substances as active pharmaceutical ingredients and reference standards for their customers. Interested parties are invited to submit comments, objections, or a request for a hearing regarding this application by April 6, 2021. Written comments should be sent to the DEA's Federal Register Representative in Springfield, Virginia.

    Simple Explanation

    Noramco Inc wants permission from the government to make special medicines from substances like Marihuana extracts. People can tell the government if they have questions or problems about this request before April 6, 2021.

  • Type:Notice
    Citation:86 FR 8220
    Reading Time:about a minute or two

    Mylan Pharmaceuticals Inc. has submitted an application to be recognized as an importer of controlled substances. The Drug Enforcement Administration (DEA), a part of the Justice Department, is providing notice of this application. Interested parties, such as other registered manufacturers or applicants, have the opportunity to submit written comments, objections, or requests for a hearing on this application by March 8, 2021. Comments and hearing requests should be sent to the DEA at their Springfield, Virginia address.

    Simple Explanation

    Mylan Pharmaceuticals wants permission to bring certain special medicines into the country, and the government wants to hear what people think about this by March 8, 2021.