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Federal Register/Vol. 85, No. 214/Wednesday, November 4 70190 Federal Register / Vol. 85, No. 214 / Wednesday, November 4, 2020 / Notices purposes of this Investigation may be Issued: October 29, 2020. DATES: Registered bulk manufacturers of disclosed to and used: (i) By the Lisa Barton, the affected basic class(es), and Commission, its employees and Offices, Secretary to the Commission. applicants therefore, may file written and contract personnel (a) for [FR Doc. 2020–24390 Filed 11–3–20; 8:45 am] comments on or objections to the developing or maintaining the records BILLING CODE 7020–02–P issuance of the proposed registration on of this or a related proceeding, or (b) in or before January 4, 2021. Such persons internal investigations, audits, reviews, may also file a written request for a and evaluations relating to the DEPARTMENT OF JUSTICE hearing on the application on or before programs, personnel, and operations of January 4, 2021. the Commission including under 5 Drug Enforcement Administration U.S.C. Appendix 3; or (ii) by U.S. ADDRESSES: Written comments should [Docket No. DEA–741] government employees and contract be sent to: Drug Enforcement personnel,2 solely for cybersecurity Administration, Attention: DEA Federal Bulk Manufacturer of Controlled Register Representative/DPW, 8701 purposes. All nonconfidential written Substances Application: Navinta LLC submissions will be available for public Morrissette Drive, Springfield, Virginia inspection at the Office of the Secretary AGENCY: Drug Enforcement 22152. and on EDIS.3 Administration, Justice. SUPPLEMENTARY INFORMATION: In ACTION: Notice of application. This action is taken under the accordance with 21 CFR 1301.33(a), this authority of section 337 of the Tariff Act SUMMARY: Navinta LLC has applied to be is notice that on September 25, 2020, of 1930, as amended (19 U.S.C. 1337), registered as a bulk manufacturer of Navinta LLC 1499 Lower Ferry Road, and of §§ 201.10 and 210.8(c) of the basic class(es) of controlled Ewing, New Jersey 08618–1414, applied Commission’s Rules of Practice and substance(s). Refer to SUPPLEMENTARY to be registered as an bulk manufacturer Procedure (19 CFR 201.10, 210.8(c)). INFORMATION listed below for further of the following basic class(es) of By order of the Commission. drug information. controlled substance(s): Controlled substance Drug code Schedule 4-Anilino-N-phenethyl-4-piperidine (ANPP) ..................................................................................................................... 8333 II Levomethorphan .............................................................................................................................................................. 9210 II Levorphanol ..................................................................................................................................................................... 9220 II Remifentanil ..................................................................................................................................................................... 9739 II Fentanyl ........................................................................................................................................................................... 9801 II The company plans to bulk DEPARTMENT OF JUSTICE comments on or objections to the manufacture active pharmaceutical issuance of the proposed registration on ingredients (API) quantities of the listed Drug Enforcement Administration or before January 4, 2021. Such persons controlled substances for validation [Docket No. DEA–717] may also file a written request for a purposes and the Food and Drug hearing on the application on or before Administration’s approval. No other Bulk Manufacturer of Controlled January 4, 2021. activity for these drug codes is Substances Application: Cerilliant ADDRESSES: Written comments should authorized for this registration. Corporation be sent to: Drug Enforcement Administration, Attention: DEA Federal AGENCY: Drug Enforcement William T. McDermott, Register Representative/DPW, 8701 Administration, Justice. Assistant Administrator. Morrissette Drive, Springfield, Virginia ACTION: [FR Doc. 2020–24465 Filed 11–3–20; 8:45 am] Notice of application. 22152. BILLING CODE 4410–09–P SUMMARY: Cerilliant Corporation has SUPPLEMENTARY INFORMATION: In applied to be registered as a bulk accordance with 21 CFR 1301.33(a), this manufacturer of basic class(es) of is notice that on August 6, 2020, controlled substance(s). Refer to Cerilliant Corporation, 811 Paloma Supplemental Information listed below Drive, Suite A, Round Rock, Texas for further drug information. 78665–2402, applied to be registered as DATES: Registered bulk manufacturers of an bulk manufacturer of the following the affected basic class(es), and basic class(es) of controlled applicants therefore, may file written substance(s): Controlled substance Drug code Schedule 3-Fluoro-N-methylcathinone (3–FMC) ............................................................................................................................. 1233 I Cathinone ........................................................................................................................................................................ 1235 I Methcathinone ................................................................................................................................................................. 1237 I 4-Fluoro-N-methylcathinone (4–FMC) ............................................................................................................................. 1238 I Pentedrone (a-methylaminovalerophenone) ................................................................................................................... 1246 I Mephedrone (4-Methyl-N-methylcathinone) .................................................................................................................... 1248 I 4-Methyl-N-ethylcathinone (4–MEC) ............................................................................................................................... 1249 I Naphyrone ....................................................................................................................................................................... 1258 I 2 All contract personnel will sign appropriate 3 Electronic Document Information System nondisclosure agreements. (EDIS): https://edis.usitc.gov. VerDate Sep<11>2014 18:16 Nov 03, 2020 Jkt 253001 PO 00000 Frm 00064 Fmt 4703 Sfmt 4703 E:\FR\FM\04NON1.SGM 04NON1 khammond on DSKJM1Z7X2PROD with NOTICES Federal Register / Vol. 85, No. 214 / Wednesday, November 4, 2020 / Notices 70191 Controlled substance Drug code Schedule N-Ethylamphetamine ....................................................................................................................................................... 1475 I N,N-Dimethylamphetamine .............................................................................................................................................. 1480 I Fenethylline ..................................................................................................................................................................... 1503 I Aminorex .......................................................................................................................................................................... 1585 I 4-Methylaminorex (cis isomer) ........................................................................................................................................ 1590 I Gamma Hydroxybutyric Acid ........................................................................................................................................... 2010 I Methaqualone .................................................................................................................................................................. 2565 I JWH–250 (1-Pentyl-3-(2-methoxyphenylacetyl)indole) ................................................................................................... 6250 I SR–18 (Also known as RCS–8) (1-Cyclohexylethyl-3-(2-methoxyphenylacetyl)indole) ................................................. 7008 I ADB–FUBINACA (N-(1-amino-3,3-dimethyl-1-oxobutan-2-yl)-1-(4-fluorobenzyl)-1H-indazole-3-carboxamide) ............. 7010 I 5-Fluoro-UR-144 and XLR11 [1-(5-Fluoro-pentyl)1H-indol-3-yl](2,2,3,3-tetramethylcyclopropyl)methanone ................. 7011 I AB–FUBINACA (N-(1-amino-3-methyl-1-oxobutan-2-yl)-1-(4-fluorobenzyl)-1H-indazole-3-carboxamide) ..................... 7012 I FUB–144 (1-(4-fluorobenzyl)-1H-indol-3-yl)(2,2,3,3-tetramethylcyclopropyl)methanone) ............................................... 7014 I JWH–019 (1-Hexyl-3-(1-naphthoyl)indole) ...................................................................................................................... 7019 I MDMB–FUBINACA (Methyl 2-(1-(4-fluorobenzyl)-1H-indazole-3-carboxamido)-3,3-dimethylbutanoate) ...................... 7020 I FUB–AMB, MMB–FUBINACA, AMB–FUBINACA (2-(1-(4-fluorobenzyl)-1Hindazole-3-carboxamido)-3- 7021 I methylbutanoate). AB–PINACA (N-(1-amino-3-methyl-1-oxobutan-2-yl)-1-pentyl-1H-indazole-3-carboxamide) ......................................... 7023 I THJ–2201 ([1-(5-fluoropentyl)-1H-indazol-3-yl](naphthalen-1-yl)methanone) ................................................................. 7024 I 5F–AB–PINACA (N-(1-amino-3-methyl-1-oxobutan-2-yl)-1-(5-fluropentyl)-1H-indazole-3-carboximide) ........................ 7025 I AB–CHMINACA
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