Bulk Manufacturer of Controlled Substances Application: S&B Pharma, Inc.; Correction, 13931 [2020-04829]

Download as PDF 13931 Federal Register / Vol. 85, No. 47 / Tuesday, March 10, 2020 / Notices Order DEPARTMENT OF JUSTICE Pursuant to 28 CFR 0.100(b) and the authority vested in me by 21 U.S.C. 824(a), I hereby revoke DEA Certificate of Registration No. FH4036667 issued to William S. Husel, D.O. Further, pursuant to 28 CFR 0.100(b) and the authority vested in me by 21 U.S.C. 823(f), I hereby deny any pending application of William S. Husel to renew or modify this registration, as well as any other applications of William S. Husel for an additional registration in Ohio. This Order is effective April 9, 2020. Drug Enforcement Administration Dated: January 29, 2020. Uttam Dhillon, Acting Administrator. [FR Doc. 2020–04837 Filed 3–9–20; 8:45 am] BILLING CODE 4410–09–P [Docket No. DEA–592] Importer of Controlled Substances Application: Johnson Matthey Inc. ACTION: Notice of application. Registered importers 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 April 9, 2020. Such persons may also file a written request for a hearing on the application on or before April 9, 2020. ADDRESSES: Written comments should be sent to: Drug Enforcement Administration, Attention: DEA Federal Register Representative/DPW, 8701 Morrissette Drive, Springfield, Virginia DATES: 22152. All requests for a hearing must be sent to: Drug Enforcement Administration, Attn: Administrator, 8701 Morrissette Drive, Springfield, Virginia 22152. All request for a 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. In accordance with 21 CFR 1301.34(a), this is notice that on September 11, 2019, Johnson Matthey Inc., Pharmaceutical Materials, 2003 Nolte Drive, West Deptford, New Jersey 08066–1742 applied to be registered as an importer of the following basic classes of controlled substances: SUPPLEMENTARY INFORMATION: Controlled substance Drug code Coca Leaves .................................................................................................................................................................... Thebaine .......................................................................................................................................................................... Opium, raw ...................................................................................................................................................................... Noroxymorophone ........................................................................................................................................................... Poppy Straw Concentrate ............................................................................................................................................... Fentanyl ........................................................................................................................................................................... The company plans to import Coca Leaves (9040), Opium, raw (9600), and Poppy Straw Concentrate (9670) in order to bulk manufacture active pharmaceutical ingredients (API) for distribution to its customers. The company plans to also import Thebaine (9333), Noroxymorophone (9668), and Fentanyl (9801) to use as analytical reference standards, both internally and to be sold to their customers to support testing of Johnson Matthey Inc.’s active pharmaceutical ingredients (API’s) only. Dated: February 10, 2020. William T. McDermott, Assistant Administrator. November 22, 2019, concerning a notice of application. As that document correctly indicated, the applicant, S&B Pharma, Inc., DBA Norac Pharma, 405 South Motor Avenue, Azusa, California 91702–3232 applied to be registered as a bulk manufacturer of a number of controlled substances, to include applying for authorization in order to synthetically manufacture using drug code 7360 (marihuana). However, on the notice of application published, drug code 7360 was inadvertently identified and listed as Gamma Hydroxybutyric Acid instead of Marihuana. SUPPLEMENTARY INFORMATION: [FR Doc. 2020–04836 Filed 3–9–20; 8:45 am] Correction BILLING CODE 4410–09–P In the Federal Register of November 22, 2019, in FR Doc. 2019–25402 (84 FR 64563), on page 64564, correct the listing of drug code 7360 to be identified as Marihuana, as is shown below. DEPARTMENT OF JUSTICE Drug Enforcement Administration khammond on DSKJM1Z7X2PROD with NOTICES [Docket No. DEA–582] Bulk Manufacturer of Controlled Substances Application: S&B Pharma, Inc.; Correction Notice of application; correction. ACTION: The Drug Enforcement Administration (DEA) published a document in the Federal Register on SUMMARY: VerDate Sep<11>2014 17:20 Mar 09, 2020 Jkt 250001 Controlled substance Drug code Schedule Marihuana ................. 7360 I Dated: February 11, 2020. William T. McDermott, Assistant Administrator. [FR Doc. 2020–04829 Filed 3–9–20; 8:45 am] BILLING CODE 4410–09–P PO 00000 Frm 00075 Fmt 4703 Sfmt 4703 9040 9333 9600 9668 9670 9801 Schedule II II II II II II DEPARTMENT OF JUSTICE Drug Enforcement Administration [Docket No. DEA–594] Importer of Controlled Substances Application: Arizona Department of Corrections ACTION: Notice of application. Registered bulk manufacturers of the affected basic class, and applicants therefore, may file written comments on or objections to the issuance of the proposed registration on or before April 9, 2020. Such persons may also file a written request for a hearing on the application on or before April 9, 2020. 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 a hearing must be sent to: Drug Enforcement Administration, Attn: Administrator, 8701 Morrissette Drive, Springfield, Virginia 22152. All requests for a 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 DATES: E:\FR\FM\10MRN1.SGM 10MRN1

Agencies

[Federal Register Volume 85, Number 47 (Tuesday, March 10, 2020)]
[Notices]
[Page 13931]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2020-04829]


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DEPARTMENT OF JUSTICE

Drug Enforcement Administration

[Docket No. DEA-582]


Bulk Manufacturer of Controlled Substances Application: S&B 
Pharma, Inc.; Correction

ACTION: Notice of application; correction.

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SUMMARY: The Drug Enforcement Administration (DEA) published a document 
in the Federal Register on November 22, 2019, concerning a notice of 
application. As that document correctly indicated, the applicant, S&B 
Pharma, Inc., DBA Norac Pharma, 405 South Motor Avenue, Azusa, 
California 91702-3232 applied to be registered as a bulk manufacturer 
of a number of controlled substances, to include applying for 
authorization in order to synthetically manufacture using drug code 
7360 (marihuana). However, on the notice of application published, drug 
code 7360 was inadvertently identified and listed as Gamma 
Hydroxybutyric Acid instead of Marihuana.

SUPPLEMENTARY INFORMATION: 

Correction

    In the Federal Register of November 22, 2019, in FR Doc. 2019-25402 
(84 FR 64563), on page 64564, correct the listing of drug code 7360 to 
be identified as Marihuana, as is shown below.

------------------------------------------------------------------------
         Controlled substance           Drug code         Schedule
------------------------------------------------------------------------
Marihuana............................       7360   I
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    Dated: February 11, 2020.
William T. McDermott,
Assistant Administrator.
[FR Doc. 2020-04829 Filed 3-9-20; 8:45 am]
 BILLING CODE 4410-09-P