[Federal Register Volume 82, Number 78 (Tuesday, April 25, 2017)]
[Notices]
[Page 19083]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2017-08343]


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DEPARTMENT OF JUSTICE

Drug Enforcement Administration

[Docket No. DEA-392]


Bulk Manufacturer of Controlled Substances Application: Cedarburg 
Pharmaceuticals

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 in accordance with 21 CFR 
1301.33(a) on or before June 26, 2017.

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

SUPPLEMENTARY INFORMATION: The Attorney General has delegated his 
authority under the Controlled Substances Act to the Administrator of 
the Drug Enforcement Administration (DEA), 28 CFR 0.100(b). Authority 
to exercise all necessary functions with respect to the promulgation 
and implementation of 21 CFR part 1301, incident to the registration of 
manufacturers, distributors, dispensers, importers, and exporters of 
controlled substances (other than final orders in connection with 
suspension, denial, or revocation of registration) has been redelegated 
to the Assistant Administrator of the DEA Diversion Control Division 
(``Assistant Administrator'') pursuant to section 7 of 28 CFR part 0, 
appendix to subpart R.
    In accordance with 21 CFR 1301.33(a), this is notice that on June 
1, 2016, Cedarburg Pharmaceuticals Inc., A Division of Albany Molecular 
Research Inc. (AMRI), 870 Badger Circle, Grafton, Wisconsin 53024 
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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Marihuana.............................      7360  I
Tetrahydrocannabinols.................      7370  I
Lisdexamfetamine......................      1205  II
4-Anilino-N-phenethyl-4-piperidine          8333  II
 (ANPP).
Remifentanil..........................      9739  II
Fentanyl..............................      9801  II
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    The company plans to manufacture the above-listed controlled 
substances in bulk for distribution to its customers. In reference to 
drug codes 7360 marihuana, the company plans to bulk manufacture 
cannabidiol as a synthetic intermediate. This controlled substance will 
be further synthesized to bulk manufacture a synthetic 
tetrahydrocannabinols 7370. No other activity for this drug code is 
authorized for this registration.

    Dated: April 18, 2017.
Louis J. Milione,
Assistant Administrator.
[FR Doc. 2017-08343 Filed 4-24-17; 8:45 am]
 BILLING CODE 4410-09-P