Manufacturer of Controlled Substances; Notice of Application

---
identifier: "/us/fr/2010-26443"
source: "fr"
legal_status: "authoritative_unofficial"
title: "Manufacturer of Controlled Substances; Notice of Application"
title_number: 0
title_name: "Federal Register"
section_number: "2010-26443"
section_name: "Manufacturer of Controlled Substances; Notice of Application"
positive_law: false
currency: "2010-10-20"
last_updated: "2010-10-20"
format_version: "1.1.0"
generator: "[email protected]"
agency: "Justice Department"
document_number: "2010-26443"
document_type: "notice"
publication_date: "2010-10-20"
agencies:
  - "Justice Department"
  - "Drug Enforcement Administration"
fr_citation: "75 FR 64744"
fr_volume: 75
---


#  Manufacturer of Controlled Substances; Notice of Application

Pursuant to § 1301.33(a) of Title 21 of the Code of Federal Regulations (CFR), this is notice that on September 14, 2010, GE Healthcare, 3350 North Ridge Avenue, Arlington Heights, Illinois 60004-1412, made application by  renewal to the Drug Enforcement Administration (DEA) as a bulk manufacturer of Cocaine (9041), a basic class of controlled substance listed in schedule II.

The company plans to manufacture a radioactive product used in diagnostic imaging in the diagnosis of Parkinson's Disease and for manufacture in bulk for investigational new drug (IND) submission and clinical trials.

Any other such applicant, and any person who is presently registered with DEA to manufacture such a substance, may file comments or objections to the issuance of the proposed registration pursuant to 21 CFR 1301.33(a).

Any such written comments or objections should be addressed, in quintuplicate, to the Drug Enforcement Administration, Office of Diversion Control, Federal Register Representative (ODL), 8701 Morrissette Drive, Springfield, VA 22152; and must be filed no later than December 20, 2010.

Dated: October 8, 2010.

Joseph T. Rannazzisi,

Deputy Assistant Administrator, Office of Diversion Control, Drug Enforcement Administration.