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Notice

Bulk Manufacturer of Controlled Substances Application: Noramco Inc.

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Start Preamble

ACTION:

Notice of application.

DATES:

Registered bulk manufacturer of the affected basic classes, and applicants therefore, may file written comments on or objections to the issuance of the proposed registration on or before January 6, 2020.

ADDRESSES:

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

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SUPPLEMENTARY INFORMATION:

In accordance with 21 CFR 1301.33(a), this is notice that on August 6, 2019, Noramco Inc., 500 Swedes Landing Road, Wilmington, Delaware 19801-4417 applied to be registered as a bulk manufacturer of the following basic classes of controlled substances:

Controlled substanceDrug codeSchedule
Marihuana7360I
Tetrahydrocannabinols7370I
Codeine-N-oxide9053I
Dihydromorphine9145I
Hydromorphinol9301I
Morphine-N-oxide9307I
Amphetamine1100II
Methylphenidate1724II
Nabilone7379II
Phenylacetone8501II
Codeine9050II
Dihydrocodeine9120II
Oxycodone9143II
Hydromorphone9150II
Hydrocodone9193II
Morphine9300II
Oripavine9330II
Thebaine9333II
Opium extracts9610II
Opium fluid extract9620II
Opium tincture9630II
Opium, powdered9639II
Opium, granulated9640II
Oxymorphone9652II
Noroxymorphone9668II
Tapentadol9780II

The company plans to manufacture the listed controlled substances as an Active Pharmaceutical Ingredient (API) for supply to its customers. In reference to drug codes 7360 (marihuana) and 7370 (tetrahydrocannabinols), the company plans to bulk manufacture these drugs as synthetics. No other activities for these drug codes are authorized for this registration.

Start Signature

Dated: October 22, 2019.

William T. McDermott,

Assistant Administrator.

End Signature End Supplemental Information

[FR Doc. 2019-24106 Filed 11-4-19; 8:45 am]

BILLING CODE 4410-09-P