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Bulk Manufacturer of Controlled Substances Application: Organic Consultants, Inc.

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Information about this document as published in the Federal Register.

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Notice of application.


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 September 25, 2017.


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

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The Attorney General has delegated his 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 Assistant Administrator of the DEA Diversion Control Division (“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 November 2, 2016, Organic Consultants, Inc., 90 North Polk Street, Suite 200, Eugene, Oregon 97402 applied to be registered as a bulk manufacturer for methadone intermediate (9254), a basic class of controlled substance listed in schedule II.

The company plans to manufacture analytical reference standards for distribution to its customers for research and analytical purposes.

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Dated: July 19, 2017.

Demetra Ashley,

Acting Assistant Administrator.

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[FR Doc. 2017-15690 Filed 7-25-17; 8:45 am]