[Federal Register Volume 84, Number 165 (Monday, August 26, 2019)]
[Notices]
[Pages 44639-44640]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2019-18324]


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DEPARTMENT OF JUSTICE

Drug Enforcement Administration

[Docket No. DEA-392]


Bulk Manufacturer of Controlled Substances Application: Cambrex 
High Point, Inc.

ACTION: Notice of application.

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DATES: Registered bulk manufacturers of the affected basic classes, and

[[Page 44640]]

applicants therefore, may file written comments on or objections to the 
issuance of the proposed registration on or before October 25, 2019.

ADDRESS:  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 19, 2019, Cambrex High Point, Inc., 4180 
Mendenhall Oaks Parkway, High Point, North Carolina 27265-8017 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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Oxymorphone............................     9652  II
Noroxymorphone.........................     9668  II
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    The company plans to manufacture the above listed controlled 
substances in bulk for distribution to its customers. No other 
activities for these drug codes are authorized for this registration.

    Dated: August 9, 2019.
Neil D. Doherty,
Acting Assistant Administrator.
[FR Doc. 2019-18324 Filed 8-23-19; 8:45 am]
 BILLING CODE 4410-09-P