Importer of Controlled Substances Application: Chattem Chemicals, Inc., 46716-46717 [2021-17764]

Download as PDF 46716 Federal Register / Vol. 86, No. 158 / Thursday, August 19, 2021 / Notices Commission is properly sought will be treated accordingly. All information, including confidential business information and documents for which confidential treatment is properly sought, submitted to the Commission for purposes of this Investigation may be disclosed to and used: (i) By the Commission, its employees and Offices, and contract personnel (a) for developing or maintaining the records of this or a related proceeding, or (b) in internal investigations, audits, reviews, and evaluations relating to the programs, personnel, and operations of the Commission including under 5 U.S.C. Appendix 3; or (ii) by U.S. government employees and contract personnel, solely for cybersecurity purposes. All contract personnel will sign appropriate nondisclosure agreements. All nonconfidential written submissions will be available for public inspection on EDIS. This action is taken under the authority of section 337 of the Tariff Act of 1930, as amended (19 U.S.C. 1337), and Part 210 of the Commission’s Rules of Practice and Procedure (19 CFR part 210). By order of the Commission. Issued: August 16, 2021. Lisa Barton, Secretary to the Commission. [FR Doc. 2021–17816 Filed 8–18–21; 8:45 am] BILLING CODE 7020–02–P DEPARTMENT OF JUSTICE Drug Enforcement Administration [Docket No. DEA–887] Importer of Controlled Substances Application: Galephar Pharmaceutical Research Inc. lotter on DSK11XQN23PROD with NOTICES1 17:28 Aug 18, 2021 Jkt 253001 Hydromorphone .............. Schedule I 9150 III The company plans to import the listed controlled substance in finished dosage form for analytical purpose only. No other activity for this drug code is authorized for this registration. Approval of permit applications will occur only when the registrant’s business activity is consistent with what is authorized under 21 U.S.C. 952(a)(2). Authorization will not extend to the import of Food and Drug Administration-approved or nonapproved finished dosage forms for commercial sale. Brian S. Besser, Acting Assistant Administrator. BILLING CODE 4410–09–P Galephar has applied to be registered as an importer of basic class(es) of controlled substance(s). Refer to SUPPLEMENTARY INFORMATION listed below for further drug information. DATES: Registered bulk manufacturers of the affected basic class(es), and applicants therefore, may file written comments on or objections to the issuance of the proposed registration on or before September 20, 2021. Such persons may also file a written request for a hearing on the application on or before September 20, 2021. ADDRESSES: Written comments should be sent to: Drug Enforcement VerDate Sep<11>2014 Drug code Controlled substance [FR Doc. 2021–17765 Filed 8–18–21; 8:45 am] Drug Enforcement Administration, Justice. ACTION: Notice of application. AGENCY: SUMMARY: 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 Representative/DPW, 8701 Morrissette Drive, Springfield, Virginia 22152. SUPPLEMENTARY INFORMATION: In accordance with 21 CFR 1301.34(a), this is notice that on July 23, 2021, Galephar Pharmaceutical Research Inc., 100 Carr 198 Industrial Park, Juncos, Puerto Rico 00777–3873, applied to be registered as an importer of the following basic class(es) of controlled substance(s): DEPARTMENT OF JUSTICE Drug Enforcement Administration [Docket No. DEA–886] Importer of Controlled Substances Application: Chattem Chemicals, Inc. Drug Enforcement Administration, Justice. ACTION: Notice of application. AGENCY: Chattem Chemicals, Inc., has applied to be registered as an importer of basic class(es) of controlled substance(s). Refer to SUPPLEMENTARY INFORMATION listed below for further drug information. SUMMARY: PO 00000 Frm 00044 Fmt 4703 Sfmt 4703 Registered bulk manufacturers of the affected basic class(es), and applicants therefore, may file written comments on or objections to the issuance of the proposed registration on or before September 20, 2021. Such persons may also file a written request for a hearing on the application on or before September 20, 2021. DATES: 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 Representative/DPW, 8701 Morrissette Drive, Springfield, Virginia 22152. ADDRESSES: In accordance with 21 CFR 1301.34(a), this is notice that on July 23, 2021, Chattem Chemicals, Inc., 3801 Saint Elmo Avenue, Chattanooga, Tennessee 37409–1237, applied to be registered as an importer of the following basic class(es) of controlled substance(s): SUPPLEMENTARY INFORMATION: Controlled substance Methamphetamine ........... 4-Anilino-N-Phenethyl-4Piperidine (ANPP). Phenylacetone ................. Coca Leaves ................... Opium, Raw ..................... Poppy Straw Concentrate Tapentadol ...................... Drug code Schedule 1105 8333 II II 8501 9040 9600 9670 9780 II II II II II The company plans to import the listed controlled substances to manufacture bulk controlled substances for sale to its customers. The company plans to import an intermediate of Tapentadol (9780), to bulk manufacture Tapentadol for distribution to its customers. No other activity for this drug code is authorized for this registration. Approval of permit applications will occur only when the registrant’s business activity is consistent with what is authorized under 21 U.S.C. 952(a)(2). Authorization will not extend to the import of Food and Drug Administration-approved or non- E:\FR\FM\19AUN1.SGM 19AUN1 Federal Register / Vol. 86, No. 158 / Thursday, August 19, 2021 / Notices approved finished dosage forms for commercial sale. Brian S. Besser, Acting Assistant Administrator. [FR Doc. 2021–17764 Filed 8–18–21; 8:45 am] BILLING CODE P DEPARTMENT OF LABOR Office of Disability Employment Policy Agency Information Collection Activities; Comment Request; Job Accommodation Network Customer Satisfaction Questionnaire Notice of information collections and request for comments. lotter on DSK11XQN23PROD with NOTICES1 ACTION: SUMMARY: In compliance with the Paperwork Reduction Act of 1995, the DOL is soliciting public comments regarding this ODEP-sponsored information collection to the Office of Management and Budget (OMB) for review and approval. DATES: Comments pertaining to this information collection are due on or before October 18, 2021. ADDRESSES: Electronic submission: You may submit comments and attachments electronically at https:// www.regulations.gov. Follow the online instructions for submitting comments. Mail submission: 200 Constitution Ave. NW, Room S–5315, Washington, DC 20210. Comments are invited on: (1) Whether the collection of information is necessary for the proper performance of the functions of the DOL, including whether the information will have practical utility; (2) if the information will be processed and used in a timely manner; (3) the accuracy of the DOL’s estimates of the burden and cost of the collection of information, including the validity of the methodology and assumptions used; (4) ways to enhance the quality, utility and clarity of the information collection; and (5) ways to minimize the burden of the collection of information on those who are to respond, including the use of automated collection techniques or other forms of information technology. FOR FURTHER INFORMATION CONTACT: Betsy Kravitz by telephone at 202–693– 7860 (this is not a toll-free number) or by email at DOL_PRA_PUBLIC@dol.gov. SUPPLEMENTARY INFORMATION: The Job Accommodation Network (JAN) is a leading source of guidance on job accommodations and disability employment issues and has served customers for more than 35 years. JAN provides free one-on-one practical guidance and technical assistance on job VerDate Sep<11>2014 17:28 Aug 18, 2021 Jkt 253001 accommodation solutions, Title I of the Americans with Disabilities Act (ADA) and related legislation, and selfemployment and entrepreneurship options for people with disabilities. JAN provides individualized consultation to assist: • Employers and their representatives seeking guidance on practical ways to engage in the interactive process, provide job accommodation solutions, and comply with Title I of the ADA; • Individuals with medical conditions and disabilities seeking information about job accommodation solutions, employment rights under the ADA, and self-employment and entrepreneurship opportunities; and • Family members and rehabilitation, medical, educational, and other professionals in their effort to support successful employment outcomes for individuals with medical conditions and disabilities. JAN customers (employer representatives, service providers, and individuals with disabilities) who contact JAN via phone calls, email, and internet chats and who have inquiries related to workplace accommodation or self-employment issues will be asked to participate in the Customer Satisfaction Questionnaire, which is sent via email. The initial email requesting participation includes the Informed Consent script used by both JAN and the West Virginia University School of Social Work. Informed consent specifies that the purpose is to evaluate JAN’s services and to identify ways in which services can be improved to assist clients. Potential participants also will be informed that their decision to either participate or refuse to participate will in no way impact their ability to use JAN’s services in the future. Following the link to complete the questionnaire is considered consent. Customers can also opt out of further contacts or choose to contact the evaluator directly if there are questions or concerns. The statement has been approved by the West Virginia University Internal Review Board. The questionnaire requests demographic information, accommodation process details and costs, and general satisfaction items. Respondents can choose to answer or skip each item. This information collection is subject to the Paperwork Reduction Act (PRA). A Federal agency generally cannot conduct or sponsor a collection of information, and the public is generally not required to respond to an information collection, unless the OMB approves it and displays a currently valid OMB Control Number. In addition, notwithstanding any other provisions of law, no person shall generally be subject PO 00000 Frm 00045 Fmt 4703 Sfmt 4703 46717 to penalty for failing to comply with a collection of information that does not display a valid OMB Control Number. See 5 CFR 1320.5(a) and 1320.6. The DOL seeks PRA authorization for this information collection for three (3) years. OMB authorization for an Information Collection Review cannot be for more than three (3) years without renewal. The DOL notes that currently approved information collection requirements submitted to the OMB receive a month-to-month extension while they undergo review. Agency: DOL–ODEP. Type of Review: New information collection. Title of Collection: Job Accommodation Network (JAN) Customer Satisfaction Questionnaire. OMB Control Number: 1230–0NEW. Affected Public: Individuals or Households. Total Estimated Number of Respondents: 1,680. Frequency: Once per customer every 6 months. Total Estimated Number of Responses: 1,680. Total Estimated Annual Time Burden: 420 hours. Total Estimated Annual Other Costs Burden: $0. Authority: 44 U.S.C. 3506(c)(2)(A). Dated: August 12, 2021. Jennifer Sheehy, Deputy Assistant Secretary, Office of Disability Employment Policy. [FR Doc. 2021–17787 Filed 8–18–21; 8:45 am] BILLING CODE 4510–FK–P DEPARTMENT OF LABOR Employment and Training Administration Determinations Regarding Eligibility To Apply for Trade Adjustment Assistance In accordance with Sections 223 and 284 (19 U.S.C. 2273 and 2395) of the Trade Act of 1974 (19 U.S.C. 2271, et seq.) (‘‘Act’’), as amended, the Department of Labor herein presents summaries of determinations regarding eligibility to apply for trade adjustment assistance under Chapter 2 of the Act (‘‘TAA’’) for workers by (TA–W) issued during the period of July 1 2021 through July 31 2021. This notice includes summaries of initial determinations such as Affirmative Determinations of Eligibility, Negative Determinations of Eligibility, and Determinations Terminating Investigations of Eligibility within the period. If issued in the E:\FR\FM\19AUN1.SGM 19AUN1

Agencies

[Federal Register Volume 86, Number 158 (Thursday, August 19, 2021)]
[Notices]
[Pages 46716-46717]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2021-17764]


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DEPARTMENT OF JUSTICE

Drug Enforcement Administration

[Docket No. DEA-886]


Importer of Controlled Substances Application: Chattem Chemicals, 
Inc.

AGENCY: Drug Enforcement Administration, Justice.

ACTION: Notice of application.

-----------------------------------------------------------------------

SUMMARY: Chattem Chemicals, Inc., has applied to be registered as an 
importer of basic class(es) of controlled substance(s). Refer to 
Supplementary Information listed below for further drug information.

DATES: Registered bulk manufacturers of the affected basic class(es), 
and applicants therefore, may file written comments on or objections to 
the issuance of the proposed registration on or before September 20, 
2021. Such persons may also file a written request for a hearing on the 
application on or before September 20, 2021.

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 Representative/DPW, 8701 Morrissette Drive, 
Springfield, Virginia 22152.

SUPPLEMENTARY INFORMATION: In accordance with 21 CFR 1301.34(a), this 
is notice that on July 23, 2021, Chattem Chemicals, Inc., 3801 Saint 
Elmo Avenue, Chattanooga, Tennessee 37409-1237, applied to be 
registered as an importer of the following basic class(es) of 
controlled substance(s):

------------------------------------------------------------------------
                                           Drug
          Controlled substance             code          Schedule
------------------------------------------------------------------------
Methamphetamine.........................    1105  II
4-Anilino-N-Phenethyl-4-Piperidine          8333  II
 (ANPP).
Phenylacetone...........................    8501  II
Coca Leaves.............................    9040  II
Opium, Raw..............................    9600  II
Poppy Straw Concentrate.................    9670  II
Tapentadol..............................    9780  II
------------------------------------------------------------------------

The company plans to import the listed controlled substances to 
manufacture bulk controlled substances for sale to its customers. The 
company plans to import an intermediate of Tapentadol (9780), to bulk 
manufacture Tapentadol for distribution to its customers. No other 
activity for this drug code is authorized for this registration.
    Approval of permit applications will occur only when the 
registrant's business activity is consistent with what is authorized 
under 21 U.S.C. 952(a)(2). Authorization will not extend to the import 
of Food and Drug Administration-approved or non-

[[Page 46717]]

approved finished dosage forms for commercial sale.

Brian S. Besser,
Acting Assistant Administrator.
[FR Doc. 2021-17764 Filed 8-18-21; 8:45 am]
BILLING CODE P
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