[Federal Register Volume 86, Number 192 (Thursday, October 7, 2021)]
[Notices]
[Pages 55859-55860]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2021-21876]


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DEPARTMENT OF JUSTICE

Drug Enforcement Administration

[Docket No. DEA-905]


Importer of Controlled Substances Application: AndersonBrecon, 
Inc.

AGENCY: Drug Enforcement Administration, Justice.

ACTION: Notice of application.

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SUMMARY: AndersonBrecon, Inc. 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 November 8, 
2021. Such persons may also file a written request for a hearing on the 
application on or before November 8, 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 
request for a hearing should also be sent to: (1) Drug

[[Page 55860]]

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 May 19, 2021, AndersonBrecon, Inc., 4545 Assembly 
Drive, Rockford, Illonois 61109, applied to be registered as an 
importer of the following basic class(es) of controlled substance(s):

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                                          Drug
          Controlled substance            code           Schedule
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Tetrahydrocannabinols..................    7370  I
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    The company plans to import the listed controlled substance for 
clinical trials only. 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.

Brian S. Besser,
Acting Assistant Administrator.
[FR Doc. 2021-21876 Filed 10-6-21; 8:45 am]
BILLING CODE 4410-09-P