Bulk Manufacturer of Controlled Substances Application: Siegfried USA, LLC

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Federal RegisterJan 12, 2021
86 Fed. Reg. 2458 (Jan. 12, 2021)

AGENCY:

Drug Enforcement Administration, Justice.

ACTION:

Notice of application.

SUMMARY:

Siegfried USA, LLC has applied to be registered as a bulk manufacturer of basic class(es) of controlled substance(s). Refer to Supplemental 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 March 15, 2021. Such persons may also file a written request for a hearing on the application on or before March 15, 2021.

ADDRESSES:

Written comments should be sent to: Drug Enforcement Administration, Attention: DEA Federal Register Representative/DPW, 8701 Morrissette Drive, Springfield, Virginia 22152.

SUPPLEMENTARY INFORMATION:

In accordance with 21 CFR 1301.33(a), this is notice that on December 9, 2020, Siegfried USA, LLC, 33 Industrial Park Road, Pennsville, New Jersey 08070-3244, applied to be registered as an bulk manufacturer of the following basic class(es) of controlled substance(s):

Controlled substance Drug code Schedule
Gamma Hydroxybutyric Acid 2010 I
Amphetamine 1100 II
Methylphenidate 1724 II
Amobarbital 2125 II
Pentobarbital 2270 II
Secobarbital 2315 II
Codeine 9050 II
Oxycodone 9143 II
Hydromorphone 9150 II
Hydrocodone 9193 II
Methadone 9250 II
Methadone intermediate 9254 II
Morphine 9300 II
Oripavine 9330 II
Thebaine 9333 II
Opium tincture 9630 II
Oxymorphone 9652 II
Tapentadol 9780 II

The company plans to bulk manufacture the listed controlled substances in bulk for sale to its customers. No other activities for these drug codes are authorized for this registration.

William T. McDermott,

Assistant Administrator.

[FR Doc. 2021-00354 Filed 1-11-21; 8:45 am]

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