What is required for a manufacturer or distributor of controlled substances?

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Study for the Federal Pharmacy Law Exam with flashcards and multiple-choice questions. Each question comes with hints and detailed explanations to enhance your understanding and readiness for the exam.

A manufacturer or distributor of controlled substances must register with the Drug Enforcement Administration (DEA) using the DEA Form 225. This form is specifically designed for entities that engage in the manufacturing or distribution of controlled substances. To maintain regulatory compliance, these businesses are required to complete this registration to legally handle controlled substances, ensuring that they are adequately monitored and that their activities align with federal laws regarding controlled substances.

In contrast, the DEA Form 224 is used by retail pharmacies, hospitals, and practitioners who dispense controlled substances. The DEA Form 363 is pertinent to narcotic treatment programs or facilities that engage in the prescribing or dispensing of narcotic drugs for the treatment of addiction. The DEA Form 106 is dedicated to reporting theft or loss of controlled substances and is not a registration form but rather a means to inform the DEA of any incidents involving the security of controlled substances.

By using the correct form, manufacturers and distributors comply with federal regulations, which helps prevent illegal diversion of controlled substances into the illicit market.

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