86 FR 234 pgs. 70147-70148 - Importer of Controlled Substances Application: Fresenius Kabi USA, LLC
Type: NOTICEVolume: 86Number: 234Pages: 70147 - 70148
Pages: 70147, 70148Docket number: [Docket No. DEA 937]
FR document: [FR Doc. 2021-26677 Filed 12-8-21; 8:45 am]
Agency: Justice Department
Sub Agency: Drug Enforcement Administration
Official PDF Version: PDF Version
[top]
DEPARTMENT OF JUSTICE
Drug Enforcement Administration
[Docket No. DEA 937]
Importer of Controlled Substances Application: Fresenius Kabi USA, LLC
AGENCY:
Drug Enforcement Administration, Justice.
ACTION:
Notice of application.
SUMMARY:
Fresenius Kabi USA, LLC has applied to be registered as an importer of basic class(es) of controlled substance(s). Refer to Supplemental Information listed below for further drug information.
DATES:
[top] Registered bulk manufacturers of the affected basic class(es), and
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 September 8, 2021, Fresenius Kabi USA, LLC, 3159 Staley Road, Grand Island, New York 14072-2028, applied to be registered as an importer of the following basic class of controlled substance:
| Controlled substance | Drug code | Schedule |
|---|---|---|
| Remifentanil | 9739 | II |
The company plans to import the listed controlled substances for bulk manufacture. 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-approved finished dosage forms for commercial sale.
Brian S. Besser,
Acting Assistant Administrator.
[FR Doc. 2021-26677 Filed 12-8-21; 8:45 am]
BILLING CODE P