Notice2025-07282
Bulk Manufacturer of Controlled Substances Application: Siemens Healthcare Diagnostics Inc.
Primary source
Metadata and text below are from the Federal Register, a public-domain U.S. government work. Always verify the official published version before relying on it for any legal matter.
Published
April 28, 2025
Issuing agencies
Justice DepartmentDrug Enforcement Administration
Abstract
Siemens Healthcare Diagnostics, Inc. has applied to be registered as a bulk manufacturer of basic class(es) of controlled substance(s). Refer to Supplementary Information listed below for further drug information.
Full Text
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<title>Federal Register, Volume 90 Issue 80 (Monday, April 28, 2025)</title>
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[Federal Register Volume 90, Number 80 (Monday, April 28, 2025)]
[Notices]
[Page 17626]
From the Federal Register Online via the Government Publishing Office [<a href="http://www.gpo.gov">www.gpo.gov</a>]
[FR Doc No: 2025-07282]
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DEPARTMENT OF JUSTICE
Drug Enforcement Administration
[Docket No. DEA-1518]
Bulk Manufacturer of Controlled Substances Application: Siemens
Healthcare Diagnostics Inc.
AGENCY: Drug Enforcement Administration, Justice.
ACTION: Notice of application.
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SUMMARY: Siemens Healthcare Diagnostics, Inc. has applied to be
registered as a bulk manufacturer 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 submit electronic comments on or
objections to the issuance of the proposed registration on or before
June 27, 2025. Such persons may also file a written request for a
hearing on the application on or before June 27, 2025.
ADDRESSES: The Drug Enforcement Administration requires that all
comments be submitted electronically through the Federal eRulemaking
Portal, which provides the ability to type short comments directly into
the comment field on the web page or attach a file for lengthier
comments. Please go to <a href="https://www.regulations.gov">https://www.regulations.gov</a> and follow the
online instructions at that site for submitting comments. Upon
submission of your comment, you will receive a Comment Tracking Number.
Please be aware that submitted comments are not instantaneously
available for public view on <a href="https://www.regulations.gov">https://www.regulations.gov</a>. If you have
received a Comment Tracking Number, your comment has been successfully
submitted and there is no need to resubmit the same comment.
SUPPLEMENTARY INFORMATION: In accordance with 21 CFR 1301.33(a), this
is notice that on January 15, 2025, Siemens Healthcare Diagnostics,
Inc., 100 GBC Drive, Mailstop 108, Newark, Delaware 19702-2461, applied
to be registered as a bulk manufacturer of the following basic
class(es) of controlled substance(s):
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Drug
Controlled substance code Schedule
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Ecgonine................................ 9180 II
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The company plans to bulk manufacture the listed controlled
substance in bulk to be used in the manufacture of the DEA exempt
products. No other activity for this drug code is authorized for this
registration.
Matthew Strait,
Deputy Assistant Administrator.
[FR Doc. 2025-07282 Filed 4-25-25; 8:45 am]
BILLING CODE 4410-09-P
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</html>Indexed from Federal Register on April 28, 2025.
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