80 FR 22556 - Importer of Controlled Substances Application: Rhodes Technologies
DEPARTMENT OF JUSTICE
Drug Enforcement Administration Federal Register Volume 80, Issue 77 (April 22, 2015)
Drug Enforcement Administration
Federal Register Volume 80, Issue 77 (April 22, 2015)
| Page Range | 22556-22556 | |
| FR Document | 2015-09338 |
[Federal Register Volume 80, Number 77 (Wednesday, April 22, 2015)] [Notices] [Page 22556] From the Federal Register Online [www.thefederalregister.org] [FR Doc No: 2015-09338] ----------------------------------------------------------------------- DEPARTMENT OF JUSTICE Drug Enforcement Administration [Docket No. DEA-392] Importer of Controlled Substances Application: Rhodes Technologies 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 1301.34(a) on or before May 22, 2015. Such persons may also file a written request for a hearing on the application pursuant to 21 CFR 1301.43 on or before May 22, 2015. ADDRESSES: Written comments should be sent to: Drug Enforcement Administration, Attention: DEA Federal Register Representative/ODXL, 8701 Morrissette Drive, Springfield, Virginia 22152. Request for hearings should be sent to: Drug Enforcement Administration, Attention: Hearing Clerk/LJ, 8701 Morrissette Drive, Springfield, Virginia 22152. Comments and request for hearings on applications to import narcotic raw material are not appropriate. 72 FR 3417 (January 25, 2007). 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 Deputy Assistant Administrator of the DEA Office of Diversion Control (``Deputy 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 March 10, 2015, Rhodes Technologies, 498 Washington Street, Coventry, Rhode Island 02816 applied to be registered as an importer of the following basic classes of controlled substances: ------------------------------------------------------------------------ Controlled Substance Schedule ------------------------------------------------------------------------ Opium, raw (9600).......................... II Poppy Straw Concentrate (9670)............. II ------------------------------------------------------------------------ The company plans to import the listed controlled substances in order to bulk manufacture controlled substances in Active Pharmaceutical Ingredient (API) form. The company distributes the manufactured APIs in bulk to its customers. Dated: April 14, 2015. Joseph T. Rannazzisi, Deputy Assistant Administrator. [FR Doc. 2015-09338 Filed 4-21-15; 8:45 am] BILLING CODE 4410-09-P
![22556 Federal Register / Vol. 80, No. 77 / Wednesday, April 22, 2015 / Notices
SUPPLEMENTARY INFORMATION: The DEPARTMENT OF JUSTICE The company plans to import the
Attorney General has delegated his listed controlled substances in order to
authority under the Controlled Drug Enforcement Administration bulk manufacture controlled substances
Substances Act to the Administrator of in Active Pharmaceutical Ingredient
the Drug Enforcement Administration [Docket No. DEA–392] (API) form. The company distributes the
(DEA), 28 CFR 0.100(b). Authority to manufactured APIs in bulk to its
exercise all necessary functions with Importer of Controlled Substances customers.
respect to the promulgation and Application: Rhodes Technologies
Dated: April 14, 2015.
implementation of 21 CFR part 1301, ACTION: Notice of application. Joseph T. Rannazzisi,
incident to the registration of Deputy Assistant Administrator.
manufacturers, distributors, dispensers, DATES: Registered bulk manufacturers of [FR Doc. 2015–09338 Filed 4–21–15; 8:45 am]
importers, and exporters of controlled the affected basic classes, and BILLING CODE 4410–09–P
substances (other than final orders in applicants therefore, may file written
connection with suspension, denial, or comments on or objections to the
revocation of registration) has been issuance of the proposed registration in DEPARTMENT OF JUSTICE
redelegated to the Deputy Assistant accordance with 21 CFR 1301.34(a) on
Administrator of the DEA Office of or before May 22, 2015. Such persons Drug Enforcement Administration
Diversion Control (‘‘Deputy Assistant may also file a written request for a [Docket No. DEA–392]
Administrator’’) pursuant to section 7 of hearing on the application pursuant to
28 CFR part 0, appendix to subpart R. 21 CFR 1301.43 on or before May 22, Importer of Controlled Substances
In accordance with 21 CFR 2015. Application: Almac Clinical Services
1301.33(a), this is notice that on May 15, ADDRESSES: Written comments should Inc. (ACSI)
2014, Cambrex Charles City, 1205 11th be sent to: Drug Enforcement
Street, Charles City, Iowa 50616 applied ACTION: Notice of application.
Administration, Attention: DEA Federal
to be registered as a bulk manufacturer Register Representative/ODXL, 8701
the following basic classes of controlled DATES: Registered bulk manufacturers of
Morrissette Drive, Springfield, Virginia the affected basic classes, and
substances: 22152. Request for hearings should be applicants therefore, may file written
sent to: Drug Enforcement comments on or objections to the
Controlled substance Schedule
Administration, Attention: Hearing issuance of the proposed registration in
Amphetamine (1100) .................... II Clerk/LJ, 8701 Morrissette Drive, accordance with 21 CFR 1301.34(a) on
Lisdexamfetamine (1205) ............. II Springfield, Virginia 22152. Comments or before May 22, 2015. Such persons
Methylphenidate (1724) ................ II and request for hearings on applications may also file a written request for a
4-Anilino-N-phenethyl-4-piperidine II to import narcotic raw material are not hearing on the application pursuant to
(8333). appropriate. 72 FR 3417 (January 25, 21 CFR 1301.43 on or before May 22,
Phenylacetone (8501) .................. II 2007). 2015.
Cocaine (9041) ............................. II SUPPLEMENTARY INFORMATION: The ADDRESSES: Written comments should
Codeine (9050) ............................. II Attorney General has delegated his be sent to: Drug Enforcement
Oxycodone (9143) ........................ II authority under the Controlled Administration, Attention: DEA Federal
Hydromorphone (9150) ................ II
Substances Act to the Administrator of Register Representative/ODXL, 8701
Hydrocodone (9193) ..................... II
the Drug Enforcement Administration Morrissette Drive, Springfield, Virginia
Morphine (9300) ........................... II
Oripavine (9330) ........................... II
(DEA), 28 CFR 0.100(b). Authority to 22152. Request for hearings should be
Thebaine (9333) ........................... II
exercise all necessary functions with sent to: Drug Enforcement
Opium, raw (9600) ....................... II respect to the promulgation and Administration, Attention: Hearing
Opium extracts (9610) .................. II implementation of 21 CFR part 1301, Clerk/LJ, 8701 Morrissette Drive,
Opium fluid extract (9620) ............ II incident to the registration of Springfield, Virginia 22152.
Opium tincture (9630) .................. II manufacturers, distributors, dispensers, SUPPLEMENTARY INFORMATION: The
Opium, powdered (9639) ............. II importers, and exporters of controlled Attorney General has delegated his
Opium, granulated (9640) ............ II substances (other than final orders in authority under the Controlled
Oxymorphone (9652) ................... II connection with suspension, denial, or Substances Act to the Administrator of
Noroxymorphone (9668) .............. II revocation of registration) has been the Drug Enforcement Administration
Poppy Straw Concentrate (9670) II redelegated to the Deputy Assistant (DEA), 28 CFR 0.100(b). Authority to
Alfentanil (9737) ........................... II Administrator of the DEA Office of exercise all necessary functions with
Remifentanil (9739) ...................... II Diversion Control (‘‘Deputy Assistant respect to the promulgation and
Sufentanil (9740) .......................... II Administrator’’) pursuant to section 7 of implementation of 21 CFR part 1301,
Fentanyl (9801) ............................ II 28 CFR part 0, appendix to subpart R. incident to the registration of
In accordance with 21 CFR manufacturers, distributors, dispensers,
The company plans to manufacture 1301.34(a), this is notice that on March importers, and exporters of controlled
the listed controlled substances in bulk 10, 2015, Rhodes Technologies, 498 substances (other than final orders in
for sale to its customers, for dosage form Washington Street, Coventry, Rhode connection with suspension, denial, or
asabaliauskas on DSK5VPTVN1PROD with NOTICES
development, for clinical trials, and for Island 02816 applied to be registered as revocation of registration) has been
use in stability qualification studies. an importer of the following basic redelegated to the Deputy Assistant
classes of controlled substances: Administrator of the DEA Office of
Dated: April 14, 2015.
Diversion Control (‘‘Deputy Assistant
Joseph T. Rannazzisi, Controlled Substance Schedule Administrator’’) pursuant to section 7 of
Deputy Assistant Administrator. 28 CFR part 0, appendix to subpart R.
[FR Doc. 2015–09325 Filed 4–21–15; 8:45 am] Opium, raw (9600) ....................... II
Poppy Straw Concentrate (9670) II
In accordance with 21 CFR
BILLING CODE 4410–09–P 1301.34(a), this is notice that on March
VerDate Sep<11>2014 18:00 Apr 21, 2015 Jkt 235001 PO 00000 Frm 00084 Fmt 4703 Sfmt 4703 E:\FR\FM\22APN1.SGM 22APN1](https://thefederalregister.org/doc/80_FR_22633/page/1.svg)
Document Created: 2015-12-16 08:27:55
Document Modified: 2015-12-16 08:27:55
| 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 1301.34(a) on or before May 22, 2015. Such persons may also file a written request for a hearing on the application pursuant to 21 CFR 1301.43 on or before May 22, 2015. | |
| FR Citation | 80 FR 22556 |
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