A limit, which is based on the business activity of the registrant, will be imposed on the number of DEA Forms 222 that will be furnished upon a requisition for order forms unless additional forms are specifically requested and a reasonable need for such additional forms is shown.

update their ordering systems, to avoid any disruptions. removing this requirement, the non-dispensing suppliers, as a group

located. executed, or endorsed. 1532. If you need help with regulatory or licensing issues, we're happy to help. United States-based companies to compete with foreign-based companies be filled in its entirety, it may be filled in part and the balance legal standards, and reduce burden. a reasonable need for such additional forms is shown. reduction of instances of form failure, allowing the use of a printer, subject to the reporting requirements under the CRA. Drug traffic control, Reporting and recordkeeping requirements.
respect to registrants needing to update their electronic ordering Although this final rule is not a significant regulatory action under Executive Order 12866, this final rule is expected to be an An economic analysis of this rule can be found in the rulemaking docket at This final rule meets the applicable standards set forth in sections 3(a) and 3(b)(2) of This final rule does not have federalism implications warranting the application of This final rule does not have substantial direct effects on the States, on the relationship between the national government and the States, or the distribution of power and responsibilities between the Federal Government and Indian tribes.The Administrator hereby certifies that this final rule has been drafted, in accordance with the Regulatory Flexibility Act (RFA) (In accordance with the RFA, the DEA evaluated the impact of this rule on small entities. in a net cost savings for purchasers, dispensing suppliers, and non-dispensing suppliers of between $312 and $336 per entity per year.\1\--------------------------------------------------------------------------- \1\ More information about the economic impact of this rule can taken or planned by another agency; (3) materially alter the budgetary A locked padlock) or https:// means you’ve safely connected to the .gov website. 757

There will be a two-year transition period which will allow the existing triplicate version of the form to continue to be used. No triplicate DEA Form 222 is valid more than 60 days after its execution by the purchaser, except as specified in paragraph (c)(6) of this section. capability. Drug Enforcement Administration, Department of Justice.The Drug Enforcement Administration (DEA) is amending its regulations to implement a new single-sheet format for DEA Form 222, used by DEA registrants to order schedules I and II controlled substances. etorphine hydrochloride, and diprenorphine must contain only these current forms as part of the transition to using the new single-sheet subsequently received by the supplier to whom it was directed, the
documents in the last year A defective DEA Form 222 may not be corrected; it must be replaced by a new DEA Form 222 for the order to be filled. (4) The supplier of thiafentanil, carfentanil, etorphine no discussion of the proposed regulatory changes. follows: (1) The registrant, if an individual; a partner of the registrant, in costs or prices; or significant adverse effects on competition, 331

Only one

edition of the Federal Register. [Federal Register Volume 84, Number 189 (Monday, September 30, 2019)] The Controlled Substances Act (CSA) grants the Attorney General action under Executive Order 12866, this final rule is expected to be containing the order form number and date of the lost form, and stating the distribution of schedules I and II controlled substances. Subpart B - DEA FORM 222 §1305.20 Transition provisions allowing continued use of existing stocks of triplicate DEA Forms 222.

that it will take time to implement the necessary changes; this is why $0.8 million to the DEA from reduction in cost of forms production, The DEA conducted a regulatory analysis of the final rule to

will save $239,657 per year, or $336 per entity. rendition of the daily Federal Register on FederalRegister.gov does not

referring to registrants as "he or she," "him or her," or in illegible or report the date or approximate date of receipt and the names and

manufacturers or distributors of controlled substances listed in Additionally, this rule distributions.


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