85 FR 89 pgs. 27248-27249 - Importer of Controlled Substances Application: AndersonBrecon Inc. dba PCI of Illinois
Type: NOTICEVolume: 85Number: 89Pages: 27248 - 27249
Pages: 27248, 27249Docket number: [Docket No. DEA-641]
FR document: [FR Doc. 2020-09707 Filed 5-6-20; 8:45 am]
Agency: Justice Department
Sub Agency: Drug Enforcement Administration
Official PDF Version: PDF Version
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DEPARTMENT OF JUSTICE
Drug Enforcement Administration
[Docket No. DEA-641]
Importer of Controlled Substances Application: AndersonBrecon Inc. dba PCI of Illinois
ACTION:
Notice of application.
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 8, 2020. Such persons may also file a written request for a hearing on the application on or before June 8, 2020.
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 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:
[top] In accordance with 21 CFR 1301.34(a), this is notice that on March 20, 2020, AndersonBrecon Inc. dba PCI of Illinois, 5775 Logistics Parkway, Rockford, Illinois 61109-3608, applied to be registered as an importer of the following basic class(es) of a controlled substance:
| Controlled substance | Drug code | Schedule |
|---|---|---|
| Tetrahydrocannabinols | 7370 | I |
The company plans to import the listed controlled substance for clinical trial 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.
William T. McDermott,
Assistant Administrator.
[FR Doc. 2020-09707 Filed 5-6-20; 8:45 am]
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