85 FR 131 pgs. 41065-41066 - Importer of Controlled Substances Application: Xcelience

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Type: NOTICEVolume: 85Number: 131Pages: 41065 - 41066

Docket number: [Docket No. DEA-681]

FR document: [FR Doc. 2020-14623 Filed 7-7-20; 8:45 am]

Agency: Justice Department

Sub Agency: Drug Enforcement Administration

Official PDF Version: PDF Version

Pages: 41065, 41066

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DEPARTMENT OF JUSTICE

Drug Enforcement Administration

[Docket No. DEA-681]

Importer of Controlled Substances Application: Xcelience

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 August 7, 2020. Such persons may also file a written request for a hearing on the application on or before August 7, 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 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 May 28, 2020, Xcelience, 4901 West Grace Street, Tampa, Florida 33607-3805, applied to be registered as an Importer of the following basic class(es) of controlled substances:

Controlled substance	Drug code	Schedule
Psilocybin	7437	I
Amphetamine	1100	II

[top] The company plans to import drug code 7437 (Psilocybin), as bulk and drug code 1100 (Amphetamine), as finished dosage form for clinical trials, research, and analytical purposes. No other activity for drug code 1100 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 the Food and Drug Administration-approved or non-approved finished dosage forms for commercial sale.

William T. McDermott,

Assistant Administrator.

[FR Doc. 2020-14623 Filed 7-7-20; 8:45 am]

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