82 FR 42119 - Bulk Manufacturer of Controlled Substances Application: Stepan Company
DEPARTMENT OF JUSTICE
Drug Enforcement Administration Federal Register Volume 82, Issue 171 (September 6, 2017)
Drug Enforcement Administration
Federal Register Volume 82, Issue 171 (September 6, 2017)
| Page Range | 42119-42119 | |
| FR Document | 2017-18789 |
[Federal Register Volume 82, Number 171 (Wednesday, September 6, 2017)] [Notices] [Page 42119] From the Federal Register Online [www.thefederalregister.org] [FR Doc No: 2017-18789] ----------------------------------------------------------------------- DEPARTMENT OF JUSTICE Drug Enforcement Administration [Docket No. DEA-392] Bulk Manufacturer of Controlled Substances Application: Stepan Company ACTION: Notice of application. ----------------------------------------------------------------------- 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 November 6, 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 January 20, 2017, Stepan Company, Natural Products Dept., 100 W. Hunter Avenue, Maywood, New Jersey 07607 applied to be registered as a bulk manufacturer of the following basic classes of controlled substances: ------------------------------------------------------------------------ Drug Controlled substance code Schedule ------------------------------------------------------------------------ Cocaine................................ 9041 II Ecgonine............................... 9180 II ------------------------------------------------------------------------ The company plans to manufacture the listed controlled substances in bulk for distribution to its customers. Dated: August 28, 2017. Demetra Ashley, Acting Assistant Administrator. [FR Doc. 2017-18789 Filed 9-5-17; 8:45 am] BILLING CODE 4410-09-P
![Federal Register / Vol. 82, No. 171 / Wednesday, September 6, 2017 / Notices 42119
person licensed, registered or otherwise registration, or any pending application Controlled substance Drug Schedule
permitted, by . . . the jurisdiction in of Marcus W. Anderson for any other code
which he practices . . . to distribute, registration, be, and it hereby is, denied. Cocaine ................................... 9041 II
dispense, [or] administer . . . a This Order is effective immediately.5 Ecgonine ................................. 9180 II
controlled substance in the course of Dated: August 28, 2017.
professional practice.’’ 21 U.S.C. The company plans to manufacture
Chuck Rosenberg,
802(21). Second, in setting the the listed controlled substances in bulk
Acting Administrator.
requirements for obtaining a for distribution to its customers.
[FR Doc. 2017–18784 Filed 9–5–17; 8:45 am]
practitioner’s registration, Congress Dated: August 28, 2017.
BILLING CODE 4410–09–P
directed that ‘‘[t]he Attorney General Demetra Ashley,
shall register practitioners . . . if the Acting Assistant Administrator.
applicant is authorized to dispense . . .
DEPARTMENT OF JUSTICE [FR Doc. 2017–18789 Filed 9–5–17; 8:45 am]
controlled substances under the laws of
BILLING CODE 4410–09–P
the State in which [s]he practices.’’ 21 Drug Enforcement Administration
U.S.C. 823(f). Because Congress has
clearly mandated that a practitioner [Docket No. DEA–392]
DEPARTMENT OF JUSTICE
possess state authority in order to be
deemed a practitioner under the Act, Bulk Manufacturer of Controlled
Substances Application: Stepan Drug Enforcement Administration
DEA has held repeatedly that revocation
of a practitioner’s registration is the Company [Docket No. DEA–392]
appropriate sanction whenever he is no ACTION: Notice of application.
longer authorized to dispense controlled Importer of Controlled Substances
substances under the laws of the State Application: KVK–Tech, Inc.
DATES: Registered bulk manufacturers of
in which he engages in professional the affected basic classes, and ACTION: Notice of application.
practice. See, e.g., Calvin Ramsey, 76 FR applicants therefore, may file written
20034, 20036 (2011); Sheran Arden comments on or objections to the DATES: Registered bulk manufacturers of
Yeates, M.D., 71 FR 39130, 39131 issuance of the proposed registration in the affected basic classes, and
(2006); Dominick A. Ricci, 58 FR 51104, accordance with 21 CFR 1301.33(a) on applicants therefore, may file written
51105 (1993); Bobby Watts, 53 FR or before November 6, 2017. comments on or objections to the
11919, 11920 (1988); Blanton, 43 FR ADDRESSES: Written comments should issuance of the proposed registration in
27616 (1978). be sent to: Drug Enforcement accordance with 21 CFR 1301.34(a) on
Moreover, because ‘‘the controlling Administration, Attention: DEA Federal or before October 6, 2017. Such persons
question’’ in a proceeding brought Register Representative/DRW, 8701 may also file a written request for a
under 21 U.S.C. 824(a)(3) is whether the Morrissette Drive, Springfield, Virginia hearing on the application pursuant to
holder of a practitioner’s registration ‘‘is 22152. 21 CFR 1301.43 on or before October 6,
currently authorized to handle 2017.
controlled substances in the [S]tate,’’ SUPPLEMENTARY INFORMATION: The
Attorney General has delegated his ADDRESSES: Written comments should
Hooper, 76 FR at 71371 (quoting Anne
authority under the Controlled be sent to: Drug Enforcement
Lazar Thorn, 62 FR 12847, 12848
Substances Act to the Administrator of Administration, Attention: DEA Federal
(1997)), the Agency has also long held
the Drug Enforcement Administration Register Representative/DRW, 8701
that revocation is warranted even where
(DEA), 28 CFR 0.100(b). Authority to Morrissette Drive, Springfield, Virginia
a practitioner has lost his state authority
exercise all necessary functions with 22152. All requests for hearing must be
by virtue of the State’s use of summary
respect to the promulgation and sent to: Drug Enforcement
process and the State has yet to provide
implementation of 21 CFR part 1301, Administration, Attn: Administrator,
a hearing to challenge the suspension.
Bourne Pharmacy, 72 FR 18273, 18274 incident to the registration of 8701 Morrissette Drive, Springfield,
(2007); Wingfield Drugs, 52 FR 27070, manufacturers, distributors, dispensers, Virginia 22152. All request for hearing
27071 (1987). Thus, it is of no importers, and exporters of controlled should also be sent to: (1) Drug
consequence that the Florida State substances (other than final orders in Enforcement Administration, Attn:
Board of Medical Examiners has connection with suspension, denial, or Hearing Clerk/LJ, 8701 Morrissette
employed summary process in revocation of registration) has been Drive, Springfield, Virginia 22152; and
suspending Registrant’s state medical redelegated to the Assistant (2) Drug Enforcement Administration,
license. What is consequential is that Administrator of the DEA Diversion Attn: DEA Federal Register
Registrant is no longer currently Control Division (‘‘Assistant Representative/DRW, 8701 Morrissette
authorized to dispense controlled Administrator’’) pursuant to section 7 of Drive, Springfield, Virginia 22152.
substances in Florida, the State in 28 CFR part 0, appendix to subpart R. SUPPLEMENTARY INFORMATION: The
which he is registered. I will therefore In accordance with 21 CFR Attorney General has delegated his
order that his registration be revoked. 1301.33(a), this is notice that on January authority under the Controlled
20, 2017, Stepan Company, Natural Substances Act to the Administrator of
Order Products Dept., 100 W. Hunter Avenue, the Drug Enforcement Administration
Maywood, New Jersey 07607 applied to (DEA), 28 CFR 0.100(b). Authority to
asabaliauskas on DSKBBXCHB2PROD with NOTICES
Pursuant to the authority vested in me
by 21 U.S.C. 823(f) and 824(a), as well be registered as a bulk manufacturer of exercise all necessary functions with
as 28 CFR 0.100(b), I order that DEA the following basic classes of controlled respect to the promulgation and
Certificate of Registration No. substances: implementation of 21 CFR part 1301,
FA3645213, issued to Marcus W. incident to the registration of
5 For the same reasons that led the Florida Board
Anderson, M.D., be, and it hereby is, manufacturers, distributors, dispensers,
of Medicine to summarily suspend Registrant’s
revoked. I further order that any medical license, I find that the public interest
importers, and exporters of controlled
pending application of Marcus W. necessitates that this Order be effective substances (other than final orders in
Anderson to renew or modify the above immediately. 21 CFR 1316.67. connection with suspension, denial, or
VerDate Sep<11>2014 17:37 Sep 05, 2017 Jkt 241001 PO 00000 Frm 00064 Fmt 4703 Sfmt 4703 E:\FR\FM\06SEN1.SGM 06SEN1](https://thefederalregister.org/doc/82_FR_42290/page/1.svg)
Document Created: 2017-09-06 00:56:50
Document Modified: 2017-09-06 00:56:50
| Category | Regulatory Information | |
| Collection | Federal Register | |
| sudoc Class | AE 2.7: GS 4.107: AE 2.106: | |
| Publisher | Office of the Federal Register, National Archives and Records Administration | |
| Section | Notices | |
| Action | Notice of application. | |
| 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 November 6, 2017. | |
| FR Citation | 82 FR 42119 |
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