Bulk Manufacturer of Controlled Substances Application: Cambridge Isotope Lab; Correction, 14471 [2021-05358]

Download as PDF 14471 Federal Register / Vol. 86, No. 49 / Tuesday, March 16, 2021 / Notices from CY 2020 to CY 2021, and such that no area has a factor less than one. For PHAs operating in multiple FMR areas, HUD calculates a voucher-weighted average inflation factor based on the count of vouchers in each FMR area administered by the PHA as captured in HUD administrative data as of December 31, 2020. National Environmental Policy Act of 1969 (42 U.S.C. 4321). III. The Use of Inflation Factors DEPARTMENT OF JUSTICE HUD subsequently applies the calculated individual area inflation factors to eligible renewal funding for each PHA based on VMS leasing and cost data for the prior calendar year. Drug Enforcement Administration jbell on DSKJLSW7X2PROD with NOTICES Drug Enforcement Administration, Justice. ACTION: Notice of application; correction. AGENCY: VI. Environmental Impact This notice involves a statutorily required establishment of a rate or cost determination which does not constitute a development decision affecting the physical condition of specific project areas or building sites. Accordingly, under 24 CFR 50.19(c)(6), this notice is categorically excluded from environmental review under the Jkt 253001 BILLING CODE 4210–67–P Bulk Manufacturer of Controlled Substances Application: Cambridge Isotope Lab; Correction As explained above, inflation factors based on area FMR changes are produced for all FMR areas and applied to eligible renewal funding for each PHA. The tables showing the RFIFs, available electronically from the HUD data information page, list the inflation factors for each FMR area on a state-bystate basis. The inflation factors use the same OMB metropolitan area definitions, as revised by HUD, that are used in the FY 2021 FMRs. PHAs should refer to the Area Definitions Table on the following web page to make certain that they are referencing the correct inflation factors: https:// www.huduser.org/portal/datasets/rfif/ FY2021/FY2021_RFIF_FMR_AREA_ REPORT.pdf. The Area Definitions Table lists areas in alphabetical order by state, and the counties associated with each area. In the six New England states, the listings are for counties or parts of counties as defined by towns or cities. HUD is also releasing the data in Microsoft Excel format to assist users who may wish to use these data in other calculations. The Excel file is available at https://www.huduser.gov/portal/ datasets/rfif/rfif.html. Note that, as described earlier, the actual renewal funding inflation factor applied to agency funding will be the voucherweighted average of the FMR area factors when the PHA operates in multiple areas. 16:52 Mar 15, 2021 [FR Doc. 2021–05365 Filed 3–15–21; 8:45 am] [Docket No. DEA–709] IV. Geographic Areas and Area Definitions VerDate Sep<11>2014 Todd Richardson, General Deputy Assistant Secretary for Policy, Development and Research. The Drug Enforcement Administration (DEA) published a document in the Federal Register of September 14, 2020, concerning a notice of application. The document contained a misspelling (Isotype vs. Isotope). SUPPLEMENTARY INFORMATION: Correction In the Federal Register of September 14, 2020, in FR Doc. 2020–20160 (85 FR 56633), on page 56633–56634, correct all instances of the registrant name to read Cambridge Isotope Lab. William T. McDermott, Assistant Administrator. [FR Doc. 2021–05358 Filed 3–15–21; 8:45 am] BILLING CODE 4410–09–P DEPARTMENT OF JUSTICE Drug Enforcement Administration [Docket No. DEA–805] Importer of Controlled Substances Application: Purisys, LLC Drug Enforcement Administration, Justice. ACTION: Notice of application. AGENCY: Purisys, LLC has applied to be registered as an importer of basic class(es) of controlled substance(s). Refer to Supplementary Information listed below for further drug information. SUMMARY: Registered bulk manufacturers of the affected basic class(es), and applicants therefore, may file written comments on or objections to the issuance of the proposed registration on or before April 15, 2021. Such persons PO 00000 Frm 00069 Fmt 4703 Sfmt 4703 Written comments should be sent to: Drug Enforcement Administration, Attention: DEA Federal Register Representative/DPW, 8701 Morrissette Drive, Springfield, Virginia 22152. All requests for a hearing must be sent to: Drug Enforcement Administration, Attn: Administrator, 8701 Morrissette Drive, Springfield, Virginia 22152. All requests for a hearing should also be sent to: (1) Drug Enforcement Administration, Attn: Hearing Clerk/OALJ, 8701 Morrissette Drive, Springfield, Virginia 22152; and (2) Drug Enforcement Administration, Attn: DEA Federal Register Representative/DPW, 8701 Morrissette Drive, Springfield, Virginia 22152. ADDRESSES: In accordance with 21 CFR 1301.34(a), this is notice that on February 17, 2021, Purisys, LLC, 1550 Olympic Drive, Athens, Georgia 30601, applied to be registered as an importer of the following basic class(es) of controlled substance(s): SUPPLEMENTARY INFORMATION: SUMMARY: DATES: may also file a written request for a hearing on the application on or before April 15, 2021. Marihuana Extract ............. Marihuana ......................... Tetrahydrocannabinols ..... Noroxymorphone .............. Phenylacetone .................. Levorphanol ...................... Thebaine ........................... Poppy Straw Concentrate Tapentadol ........................ 7350 7360 7370 7379 8501 9220 9333 9670 9780 I I I II II II II II II The company plans to import drug code 8501, Phenylacetone and drug code 9670, Poppy Straw Concentrate to bulk manufacture other controlled substances for distribution to its customers. The company plans to import impurities of buprenorphine that have been determined by DEA to be captured under drug code 9333, Thebaine. In reference to drug codes 73760, Marihuana and 7370, Tetrahydrocannabinols the company plans to import a Synthetic Cannabidiol and a Synthetic Tetrahydrocannabinol. No other activity for these drug codes is authorized for this registration. Placement of these drug codes on the company’s registration does not translate into automatic approval of subsequent permit applications to import controlled substances. Approval of permit applications will occur only when the registrant’s business activity is consistent with what is authorized under 21 U.S.C. 952(a)(2). Authorization will not extend to the import of Food and Drug Administration-approved or non- E:\FR\FM\16MRN1.SGM 16MRN1

Agencies

[Federal Register Volume 86, Number 49 (Tuesday, March 16, 2021)]
[Notices]
[Page 14471]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2021-05358]


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DEPARTMENT OF JUSTICE

Drug Enforcement Administration

[Docket No. DEA-709]


Bulk Manufacturer of Controlled Substances Application: Cambridge 
Isotope Lab; Correction

AGENCY: Drug Enforcement Administration, Justice.

ACTION: Notice of application; correction.

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SUMMARY: The Drug Enforcement Administration (DEA) published a document 
in the Federal Register of September 14, 2020, concerning a notice of 
application. The document contained a misspelling (Isotype vs. 
Isotope).

SUPPLEMENTARY INFORMATION: 

Correction

    In the Federal Register of September 14, 2020, in FR Doc. 2020-
20160 (85 FR 56633), on page 56633-56634, correct all instances of the 
registrant name to read Cambridge Isotope Lab.

William T. McDermott,
Assistant Administrator.
[FR Doc. 2021-05358 Filed 3-15-21; 8:45 am]
BILLING CODE 4410-09-P

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