Importer of Controlled Substances Application: VHG Labs DBA LGC Standards, 23740 [2021-09302]

Download as PDF 23740 Federal Register / Vol. 86, No. 84 / Tuesday, May 4, 2021 / Notices 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 nonapproved finished dosage forms for commercial sale. DEPARTMENT OF JUSTICE Drug Enforcement Administration [Docket No. DEA–831] Importer of Controlled Substances Application: VHG Labs DBA LGC Standards Drug Enforcement Administration, Justice. ACTION: Notice of application. AGENCY: William T. McDermott, Assistant Administrator. VHG Labs DBA LGC Standards has applied to be registered as an importer of basic class(es) of controlled substance(s). Refer to Supplemental Information listed below for further drug information. DATES: 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 June 3, 2021. Such persons may also file a written request for a hearing on the application on or before June 3, 2021. ADDRESSES: 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. SUPPLEMENTARY INFORMATION: In accordance with 21 CFR 1301.34(a), this is notice that on April 21, 2021, VHG Labs DBA LGC Standards, 3 Perimeter Road, Manchester, New Hampshire 03103, applied to be registered as an importer of the following basic class(es) of controlled substance(s): khammond on DSKJM1Z7X2PROD with NOTICES SUMMARY: [FR Doc. 2021–09302 Filed 5–3–21; 8:45 am] BILLING CODE P DEPARTMENT OF JUSTICE Drug Enforcement Administration [Docket No. DEA–828] Importer of Controlled Substances Application: Wildlife Laboratories, LLC Drug Enforcement. Administration, Justice. ACTION: Notice of application. AGENCY: VerDate Sep<11>2014 17:13 May 03, 2021 Jkt 253001 PO 00000 Frm 00071 Fmt 4703 Sfmt 4703 Etorphine HCl ............... Thiafentanil ................... I 9059 9729 Schedule I II II The company plans to import the listed controlled substances for distribution to its customers. No other activity for these drug codes is authorized for this registration. 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 nonapproved finished dosage forms for commercial sale. William T. McDermott, Assistant Administrator. [FR Doc. 2021–09300 Filed 5–3–21; 8:45 am] BILLING CODE P Wildlife Laboratories, LLC has applied to be registered as an importer of basic class(es) of controlled substance(s). Refer to Supplemental Information listed below for further drug information. DATES: 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 June 3, 2021. Such persons may also file a written request for a hearing on the application on or before June 3, 2021. ADDRESSES: 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 Drug Controlled substance Schedule code Drive, Springfield, Virginia 22152; and (2) Drug Enforcement Administration, Fentanyl related-comAttn: DEA Federal Register pounds as defined in Representative/DPW, 8701 Morrissette 21 CFR 1308.11(h) ... 9850 I Oxycodone .................... 9143 II Drive, Springfield, Virginia 22152. Hydromorphone ............ 9150 II SUPPLEMENTARY INFORMATION: In accordance with 21 CFR 1301.34(a), this The company plans to import the is notice that on April 8, 2021, Wildlife listed controlled substances for sale to Laboratories, LLC, 1230 W Ash Street, research facilities for drug testing and Unit D, Windsor, Colorado 80550–4677, analysis. No other activities for these applied to be registered as an importer drug codes are authorized for this of the following basic class(es) of registration. controlled substance(s): SUMMARY: Drug code Controlled substance DEPARTMENT OF JUSTICE Drug Enforcement Administration [Docket No. DEA–830] Bulk Manufacturer of Controlled Substances Application: Cargill, Incorporated Drug Enforcement Administration, Justice. ACTION: Notice of application. AGENCY: Cargill, Inc., has applied to be registered as a bulk manufacturer of basic class(es) of controlled substance(s). Refer to Supplemental Information listed below for further drug information. DATES: 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 July 6, 2021. Such persons may also file a written request for a hearing on the application on or before July 6, 2021. ADDRESSES: Written comments should be sent to: Drug Enforcement Administration, Attention: DEA Federal Register Representative/DPW, 8701 Morrissette Drive, Springfield, Virginia 22152. SUMMARY: In accordance with 21 CFR 1301.33(a), this is notice that on March 31, 2021, Cargill, Incorporated, 17540 Monroe Wapello Road, Eddyville, Iowa 52553, applied to be registered as a bulk manufacturer of the following basic class(es) of controlled substance(s): SUPPLEMENTARY INFORMATION: E:\FR\FM\04MYN1.SGM 04MYN1

Agencies

[Federal Register Volume 86, Number 84 (Tuesday, May 4, 2021)]
[Notices]
[Page 23740]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2021-09302]



[[Page 23740]]

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DEPARTMENT OF JUSTICE

Drug Enforcement Administration

[Docket No. DEA-831]


Importer of Controlled Substances Application: VHG Labs DBA LGC 
Standards

AGENCY: Drug Enforcement Administration, Justice.

ACTION: Notice of application.

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SUMMARY: VHG Labs DBA LGC Standards has applied to be registered as an 
importer of basic class(es) of controlled substance(s). Refer to 
Supplemental Information listed below for further drug information.

DATES: 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 June 3, 2021. 
Such persons may also file a written request for a hearing on the 
application on or before June 3, 2021.

ADDRESSES: 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.

SUPPLEMENTARY INFORMATION: In accordance with 21 CFR 1301.34(a), this 
is notice that on April 21, 2021, VHG Labs DBA LGC Standards, 3 
Perimeter Road, Manchester, New Hampshire 03103, applied to be 
registered as an importer of the following basic class(es) of 
controlled substance(s):

------------------------------------------------------------------------
                                                        Drug
                Controlled substance                    code    Schedule
------------------------------------------------------------------------
Fentanyl related-compounds as defined in 21 CFR          9850          I
 1308.11(h).........................................
Oxycodone...........................................     9143         II
Hydromorphone.......................................     9150         II
------------------------------------------------------------------------

    The company plans to import the listed controlled substances for 
sale to research facilities for drug testing and analysis. No other 
activities for these drug codes are authorized for this registration.
    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-approved finished 
dosage forms for commercial sale.

William T. McDermott,
Assistant Administrator.
[FR Doc. 2021-09302 Filed 5-3-21; 8:45 am]
BILLING CODE P

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