[Federal Register Volume 83, Number 247 (Thursday, December 27, 2018)]
[Notices]
[Page 66751]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2018-28081]


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DEPARTMENT OF JUSTICE

Drug Enforcement Administration

[Docket No. DEA-392]


Importer of Controlled Substances Application: Myoderm

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 January 28, 2019. 
Such persons may also file a written request for a hearing on the 
application on or before January 28, 2019.

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 
hearing must be sent to: Drug Enforcement Administration, Attn: 
Administrator, 8701 Morrissette Drive, Springfield, Virginia 22152. All 
requests for 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: 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 1301.34(a), this is notice that on 
November 2, 2018, Myoderm, 48 East Main Street, Norristown, 
Pennsylvania 19401-4915 applied to be registered as an importer of the 
following basic classes of controlled substances:

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              Controlled substance                 Drug code   Schedule
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Amphetamine.....................................        1100          II
Lisdexamfetamine................................        1205          II
Methylphenidate.................................        1724          II
Nabilone........................................        7379          II
Oxycodone.......................................        9143          II
Hydromorphone...................................        9150          II
Hydrocodone.....................................        9193          II
Morphine........................................        9300          II
Oxymorphone.....................................        9652          II
Fentanyl........................................        9801          II
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    The company plans to import the listed controlled substances for 
clinical trials, research, and analytical purposes.
    Approval of permit applications will occur only when the 
registrant's activity is consistent with what is authorized under to 21 
U.S.C.952(a)(2).
    Authorization will not extend to the import of FDA approved or non-
approved finished dosage forms for commercial sale.

    Dated: December 8, 2018.
John J. Martin,
Assistant Administrator.
[FR Doc. 2018-28081 Filed 12-26-18; 8:45 am]
BILLING CODE 4410-09-P