Tap any paragraph to write a margin note. Your notes collect in the Desk below the text and file under cases with @. The side-by-side margin rail opens on a larger screen.

Code · REGISTER · 2016-02-12 · DEPARTMENT OF JUSTICE · Notices

Notices. Notice of application

328 words·~1 min read·/register/2016/02/12/2016-02863

A research copy — for the controlling text, always check the official state or federal source. Not legal advice.

BILLING CODE 7020-02-P DEPARTMENT OF JUSTICE Drug Enforcement Administration [Docket No. DEA-392] Bulk Manufacturer of Controlled Substances Application: Noramco, Inc. ACTION: Notice of application. DATES: Registered bulk manufacturers of the affected basic classes, and applicants therefore, may file written comments on or objections to the issuance of the proposed registration in accordance with 21 CFR 1301.33(a) on or before April 12, 2016. ADDRESSES: Written comments should be sent to:
Drug Enforcement Administration, Attention: DEA Federal Register Representative/ODXL, 8701 Morrissette Drive, Springfield, Virginia 22152. SUPPLEMENTARY INFORMATION: The Attorney General has delegated her authority under the Controlled Substances Act to the Administrator of the Drug Enforcement Administration (DEA), 28 CFR 0.100(b). Authority to exercise all necessary functions with respect to the promulgation and implementation of 21 CFR part 1301, incident to the registration of manufacturers, distributors, dispensers, importers, and exporters of controlled substances (other than final orders in connection with suspension, denial, or revocation of registration) has been redelegated to the Deputy Assistant Administrator of the DEA Office of Diversion Control (“Deputy Assistant Administrator”) pursuant to section 7 of 28 CFR part 0, appendix to subpart R.
In accordance with 21 CFR 1301.33(a), this is notice that on August 4, 2015, Noramco, Inc., 1440 Olympic Drive, Athens, Georgia 30601, applied to be registered as a bulk manufacturer of the following basic classes of controlled substances: Controlled substance Schedule Gamma Hydroxybutyric Acid
(2010)I Codeine-N-oxide
(9053)I Dihydromorphine
(9145)I Morphine-N-oxide
(9307)I Amphetamine
(1100)II Methylphenidate
(1724)II Codeine
(9050)II Dihydrocodeine
(9120)II Oxycodone
(9143)II Hydromorphone
(9150)II Hydrocodone
(9193)II Morphine
(9300)II Oripavine
(9330)II Thebaine
(9333)II Opium tincture
(9630)II Oxymorphone
(9652)II Noroxymorphone
(9668)II Alfentanil
(9737)II Sufentanil
(9740)II Carfentanil
(9743)II Tapentadol
(9780)II Fentanyl
(9801)II The company plans to manufacture the listed controlled substances in bulk for distribution to its customers. Dated: January 27, 2016. Louis J. Milione, Deputy Assistant Administrator. [FR Doc. 2016-02863 Filed 2-11-16; 8:45 am]
Connectionstraces to 2
2 references not yet in our index
  • 21 CFR 1301
  • 28 CFR 0
Citation graph
cites case law
Notices
Notice of application
Cite21 CFR 1301
Cite28 CFR 0
Cites 4Cited by 0 across 0 sources
★   the supreme law of the land   ★
Don't Tread on Me
E Pluribus Unum — out of many, one

"If you don't know your rights, you don't have any."

Marginalia · a citizen's law index
A research desk, not legal advice. Always read the cited source before relying on a summary.
Questions or an issue? support@self-law.org
disclaimerMarginalia is a research index, not a law firm. Nothing on this site is legal, tax, or financial advice and no attorney–client relationship is formed by using it. Statutes, regulations, and case law change; summaries, search results, AI output, and member posts may be incomplete, out of date, or wrong. Any interpretation drawn from material on this site should be validated by a licensed attorney in your jurisdiction before you act on it.