90 FR 79 pgs. 17450-17452 - Bulk Manufacturer of Controlled Substances Application: SpecGx LLC

Type: NOTICEVolume: 90Number: 79Pages: 17450 - 17452
Docket number: [Docket No. DEA-1520]
FR document: [FR Doc. 2025-07154 Filed 4-24-25; 8:45 am]
Agency: Justice Department
Sub Agency: Drug Enforcement Administration
Official PDF Version:  PDF Version
Pages: 17450, 17451, 17452

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DEPARTMENT OF JUSTICE

Drug Enforcement Administration

[Docket No. DEA-1520]

Bulk Manufacturer of Controlled Substances Application: SpecGx LLC

AGENCY:

Drug Enforcement Administration, Justice.

ACTION:

Notice of application.

SUMMARY:


[top] SpecGx LLC has applied to be registered as a bulk manufacturer of basic class(es) of controlled page 17451 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 24, 2025. Such persons may also file a written request for a hearing on the application on or before June 24, 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 https://www.regulations.gov 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 https://www.regulations.gov. 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 February 17, 2025, SpecGx LLC, 3600 North 2nd Street, Saint Louis, Missouri 63147-3457, applied to be registered as a bulk manufacturer of the following basic class(es) of controlled substance(s):

Controlled substance Drug code Schedule
Gamma Hydroxybutyric Acid 2010 I
Tetrahydrocannabinols 7370 I
Psilocybin 7437 I
Codeine-N-oxide 9053 I
Dihydromorphine 9145 I
Difenoxin 9168 I
Morphine-N-oxide 9307 I
Normorphine 9313 I
Alphamethadol 9605 I
Betamethadol 9609 I
Norlevorphanol 9634 I
Acetyl Fentanyl (N-(1-phenethylpiperidin-4-yl)-N-phenylacetamide) 9821 I
Butyryl Fentanyl 9822 I
Fentanyl related compounds as defined in 21 CFR 1308.11(h) 9850 I
Amphetamine 1100 II
Methamphetamine 1105 II
Lisdexamfetamine 1205 II
Methylphenidate 1724 II
Nabilone 7379 II
ANPP (4-Anilino-N-phenethyl-4-piperidine) 8333 II
Phenylacetone 8501 II
Codeine 9050 II
Dihydrocodeine 9120 II
Oxycodone 9143 II
Hydromorphone 9150 II
Diphenoxylate 9170 II
Ecgonine 9180 II
Hydrocodone 9193 II
Levorphanol 9220 II
Isomethadone 9226 II
Meperidine 9230 II
Meperidine intermediate-A 9232 II
Meperidine intermediate-B 9233 II
Meperidine intermediate-C 9234 II
Methadone 9250 II
Methadone intermediate 9254 II
Dextropropoxyphene, bulk (non-dosage forms) 9273 II
Morphine 9300 II
Oripavine 9330 II
Thebaine 9333 II
Opium tincture 9630 II
Opium, powdered 9639 II
Oxymorphone 9652 II
Noroxymorphone 9668 II
Alfentanil 9737 II
Remifentanil 9739 II
Sufentanil 9740 II
Tapentadol 9780 II
Fentanyl 9801 II


[top] The company plans to bulk manufacture the listed controlled substances for sale to its customers as Active Pharmaceutical Ingredients and Analytical Research Standards for formulation and analytical development purposes. In reference to drug code 7370 (Tetrahydrocannabinols), the company plans to bulk manufacture this drug code as synthetic. No other activity for page 17452 this drug code is authorized for this registration.

Matthew Strait,

Deputy Assistant Administrator.

[FR Doc. 2025-07154 Filed 4-24-25; 8:45 am]

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