Question: Can I use a Post Office (PO) Box or Private Mailbox (PMB) address as my registered address?
Answer: Your registered address must be the physical location of your principal place of business or professional practice where controlled substances are manufactured, distributed, imported, exported, or dispensed. 21 CFR 1301.12(a). In limited circumstances, a PO Box may be included in addition to the physical business address, but a PO Box alone is not a registered address. You may, however, use a different address for your mailing address for DEA correspondence, which may be a PO Box or a PMB address. EO-DEA206, DEA-DC-050, December 12, 2020
Question: Can I change the address on my current DEA registration or do I have to get a new DEA registration for the new location?
Answer: Yes, you can change the address on your current DEA Registration. If you prefer, you can also call your Local Diversion Field Office for assistance, or you can ask a Registration Specialist for assistance by calling 1-800-882-9539 or by emailing your request to DEARegistrationHelp@usdoj.gov. EO-DEA185, November 2, 2020
Question: I live on the border between two states and I have a practice in each state. Do I need to hold a separate DEA registration number in each state?
Answer: Yes. Since DEA's authority to register practitioners to dispense (including to prescribe) controlled substances is contingent, in part, upon the applicant's authorization in the state in which he or she practices, his or her controlled substance privileges and limits are determined by that specific state. The Controlled Substances Act requires a separate registration at each principal place of business or professional practice where the controlled substances are distributed or dispensed. See 21 U.S.C. 822(e)(1), 21 CFR 1301.12(a). Therefore, a practitioner who maintains a professional practice location in multiple states has established, for registration purposes, a principal place of business in each of those states. Consequently, DEA requires that the practitioner obtain a separate DEA registration in each state. Further, to do so the practitioner must first obtain authorization to handle controlled substances in each state where he or she has an office. For additional information please see the Final Rule titled: Clarification of Registration Requirements for Individual Practitioners, which DEA published in the Federal Register on December 1, 2006. EO-DEA181, November 2, 2020
Question: Once I obtain a DEA registration can I prescribe controlled substances anywhere in the United States as it is a Federal number?
Answer: No. A DEA individual practitioner registration is based on a State license to practice medicine and prescribe controlled substances. DEA relies on State licensing boards to determine whether a practitioner is qualified to dispense, prescribe, or administer controlled substances and to determine which schedules he/she may dispense, prescribe, or administer. State authority to conduct the above-referenced activities only confers rights and privileges within the issuing State. Thus, a DEA registration based on a State license cannot authorize controlled substance dispensing outside the State. See Registration Requirements for Individual Practitioners Operating in a "Locum Tenens" Capacity, 75 FR 55499, 55501 (Oct. 28, 2009); 21 U.S.C. 823(f); 21 CFR 1306.03(a). EO-DEA089, October 21, 2020
Question: Is a separate registration required for each principal place of business or professional practice?
Answer: Yes. 21 CFR 1301.12(a), "A separate location is required for each principal place of business or professional practice at one general physical location where controlled substances are manufactured, distributed, imported, exported, or dispensed by a person." EO-DEA090, October 9, 2020
Question: I currently have a DEA registration to import controlled substances into the United States. Do I need to obtain a separate DEA registration as a chemical importer to also import a scheduled listed chemical product (SLCP) as defined under the Combat Methamphetamine Epidemic Act of 2005 (CMEA) (i.e., pseudoephedrine, ephedrine, or phenylpropanolamine), or a drug product that contains a List I chemical?
Answer: No. Under specific circumstances a separate DEA registration as a chemical importer is not required if you hold a registration to import controlled substances. DEA regulations provide a waiver to the separate registration requirement for certain List I chemical activities if the person is already registered with DEA to import controlled substances. 21 CFR 1309.24. Specifically, any person who imports or exports an SLCP or other product containing a List I chemical described and included in the definition of a regulated transaction found at 21 CFR 1300.02(1)(iv) is not required to obtain a separate registration for those activities if already registered to import controlled substances. See 21 CFR 1309.24(c). EO-DEA225, October 5, 2020
Question: Does DEA require that a practitioner take special classes, or some type of continuing education, before they can apply for, or reapply for, a DEA registration?
Answer: No. DEA does not have any educational requirements, but individual states may have educational requirements in order to obtain and maintain a valid license in that state. DEA merely requires that all state licensing requirements be met in order to obtain a DEA registration in that state. 21 U.S.C. 823(f)(1) and (4). EO-DEA182, October 5, 2020
Question: I am a practitioner, but I never plan on administering, dispensing, or prescribing a controlled substance. Must I have a DEA registration?
Answer: No. DEA regulations require that "only persons actually engaged in" the "dispens[ing] . . . of any controlled substance" hold a registration. 21 CFR 1301.11(a); see 21 U.S.C. 802(10) (defining "dispense" to include "the prescribing and administering of a controlled substance"). EO-DEA191, June 23, 2020
Disclaimer: Guidance documents, like this document, are not binding and lack the force and effect of law, unless expressly authorized by statute or expressly incorporated into a contract, grant, or cooperative agreement. Consistent with Executive Order 13891 and the Office of Management and Budget implementing memoranda, the Department will not cite, use, or rely on any guidance document that is not accessible through the Department's guidance portal, or similar guidance portals for other Executive Branch departments and agencies, except to establish historical facts. To the extent any guidance document sets out voluntary standards (e.g., recommended practices), compliance with those standards is voluntary, and noncompliance will not result in enforcement action. Guidance documents may be rescinded or modified in the Department's complete discretion, consistent with applicable laws.