[Federal Register Volume 84, Number 208 (Monday, October 28, 2019)]
[Notices]
[Page 57748]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2019-23499]


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DEPARTMENT OF JUSTICE

Drug Enforcement Administration

[Docket No. DEA-392]


Bulk Manufacturer of Controlled Substances Application: Euticals 
Inc.

ACTION: Notice of application.

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DATES: Registered bulk manufacturers of the affected basic classes, and 
applicants therefore, may file written comments on or objections to the 
issuance of the proposed registration on or before December 27, 2019.

ADDRESSES: Written comments should be sent to: Drug Enforcement 
Administration, Attention: DEA Federal Register Representative/DPW, 
8701 Morrissette Drive, Springfield, Virginia 22152.

SUPPLEMENTARY INFORMATION: In accordance with 21 CFR 1301.33(a), this 
is notice that on June 27, 2019, Euticals Inc., 2460 W Bennett Street, 
Springfield, Missouri 65807-1229 applied to be registered as a bulk 
manufacturer of the following basic classes of controlled substances:

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                                           Drug
          Controlled substance             code          Schedule
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Gamma Hydroxybutyric Acid..............     2010  I
Amphetamine............................     1100  II
Lisdexamfetamine.......................     1205  II
Methylphenidate........................     1724  II
Phenylacetone..........................     8501  II
Methadone..............................     9250  II
Methadone intermediate.................     9254  II
Oripavine..............................     9330  II
Tapentadol.............................     9780  II
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    The company plans to manufacture the above-listed controlled 
substances in bulk for distribution to its customers.

    Dated: October 18, 2019.
William T. McDermott,
Assistant Administrator.
[FR Doc. 2019-23499 Filed 10-25-19; 8:45 am]
 BILLING CODE 4410-09-P