By Joyce Brennfleck Shannon
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Extra resources for Drug Abuse Sourcebook, Third Edition
It excludes from such definition: (1) manufacturers or distributors who do not dispense controlled substances to an unregistered individual or entity; (2) non-pharmacy practitioners; (3) certain hospitals or medical facilities operated by the federal government or by an Indian tribe or tribal organization; (4) mere advertisements that do not attempt to facilitate an actual transaction involving a controlled substance; and (5) other persons or entities the exclusion of which the Attorney General and the Secretary of Health and Human Services find to be consistent with effective controls against diversion and with the public health and safety.
What information is required on a prescription for a controlled substance? A prescription for a controlled substance must include the following information: • Date of issue • Patient’s name and address • Practitioner’s name, address, and Drug Enforcement Administration (DEA) registration number • Drug name • Drug strength • Dosage form • Quantity prescribed • Directions for use • Number of refills (if any) authorized • Manual signature of prescriber 30 Purchasing Controlled Substances A prescription must be written in ink or indelible pencil or typewritten and must be manually signed by the practitioner.
Quotas: DEA limits the quantity of schedule I and II controlled substances which may be produced in the United States in any given calendar year. The DEA establishes annual aggregate production quotas for schedule I and II controlled substances. DEA also allocates the amount of bulk drug which may be procured by those companies which prepare the drug into dosage units. Security: DEA registrants are required by regulation to maintain certain security for the storage and distribution of controlled substances.