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Drug Enforcement Administration – Federal Register Recent Federal Regulation Documents
Results 1 - 50 of 851
| Document | Doc Number | Type | Agency | |
|---|---|---|---|---|
| July 15, 2008 | ||||
| Redelegation of Functions | 40463–40464 [E8–16012] | Rule | Drug Enforcement Administration | |
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DEPARTMENT OF JUSTICE Drug Enforcement Administration 28 CFR Part 0 [Docket No. DEA-310F] Redelegation of Functions AGENCY: Drug Enforcement Administration, Department of
Justice. ACTION: Final rule. SUMMARY: This rule makes one revision to the Drug Enforcement Administration's (DEA) regulations concerning agency management. Additional personnel
are authorized to sign and issue administrative subpoenas. DATES: Effective Date: July 15, 2008. FOR FURTHER INFORMATION CONTACT: Wendy H. Goggin,... [read document] |
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| July 14, 2008 | ||||
| Electronic Prescriptions for Controlled Substances; Correction | 40451 [Z8–14405] | Proposed Rule | Drug Enforcement Administration | |
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DEPARTMENT OF JUSTICE Drug Enforcement Administration 21 CFR Parts 1300, 1304, 1306 and 1311 [Docket No. DEA-218P] RIN 1117-AA61 Electronic Prescriptions for Controlled
Substances Correction In proposed rule document E8-14405 beginning on page 36722 in the issue of Friday, June 27, 2008, make the following correction: On page 36766, in Table
18, in the third column, in the first entry, ``$167,70'' should read ``$167,270''. [FR Doc. Z8-14405 Filed 7-11-08; 8:45 am] BILLING CODE 1505-01-D [read document] |
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| Denial of Application: Randall Relyea, D.O | 40378–40380 [E8–15923] | Notice | Drug Enforcement Administration | |
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DEPARTMENT OF JUSTICE Drug Enforcement Administration Randall Relyea, D.O.; Denial of Application On July 25, 2007, the Deputy Assistant Administrator, Office of Diversion
Control, Drug Enforcement Administration, issued an Order to Show Cause to Randall Relyea, D.O. (Respondent), of Price, Utah. The Show Cause Order proposed the revocation of
Respondent's DEA Certificate of Registration, BR8899809, as a practitioner, on the ground that Respondent's ``continued registration is inconsistent with... [read document] |
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| Denial of Application: Armando B. Figueroa, M.D | 40380–40382 [E8–15922] | Notice | Drug Enforcement Administration | |
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DEPARTMENT OF JUSTICE Drug Enforcement Administration Armando B. Figueroa, M.D.; Revocation of Registration On November 14, 2007, I, the Deputy Administrator of the Drug
Enforcement Administration, issued an Order to Show Cause and Immediate Suspension of Registration to Armando B. Figueroa, M.D. (Respondent), of Washington, DC. The Order
immediately suspended and proposed the revocation of Respondent's DEA Certificate of Registration, BF0128810, as a practitioner, on the grounds that his... [read document] |
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| Denial of Application: Michael Chait, M.D | 40382–40383 [E8–15938] | Notice | Drug Enforcement Administration | |
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DEPARTMENT OF JUSTICE Drug Enforcement Administration [Docket No. 08-8] Michael Chait, M.D.; Revocation of Registration On October 1, 2007, the Deputy Assistant Administrator,
Office of Diversion Control, Drug Enforcement Administration, issued an Order to Show Cause to Michael Chait, M.D. (Respondent), of Amagansett, New York. The Show Cause Order
proposed the revocation of Respondent's DEA Certificate of Registration, BC2825151, as a practitioner, and the denial of any pending applications to... [read document] |
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| July 10, 2008 | ||||
| Elimination of Exemptions: Chemical Mixtures Containing the List I Chemicals Ephedrine and/or Pseudoephedrine | 39611–39614 [E8–15704] | Rule | Drug Enforcement Administration | |
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DEPARTMENT OF JUSTICE Drug Enforcement Administration 21 CFR Part 1310 [Docket No. DEA-284F] RIN 1117-AB11 Elimination of Exemptions for Chemical Mixtures Containing the List I
Chemicals Ephedrine and/or Pseudoephedrine AGENCY: Drug Enforcement Administration (DEA), Department of Justice. ACTION: Final rule. SUMMARY: The Drug Enforcement Administration
(DEA) is finalizing, without change, the Interim Rule with Request for Comment published in the Federal Register on July 25, 2007 (72 FR 40738).... [read document] |
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| July 1, 2008 | ||||
| Controlled Substances: 2008 Proposed Revised Aggregate Production Quotas | 37496–37498 [E8–14903] | Notice | Drug Enforcement Administration | |
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DEPARTMENT OF JUSTICE Drug Enforcement Administration [Docket No. DEA-307R] Controlled Substances: Proposed Revised Aggregate Production Quotas for 2008 AGENCY: Drug Enforcement
Administration (DEA), Justice. ACTION: Notice of proposed revised 2008 aggregate production quotas. SUMMARY: This notice proposes revised 2008 aggregate production quotas for
controlled substances in schedules I and II of the Controlled Substances Act (CSA). DATES: Written comments must be postmarked, and electronic... [read document] |
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| June 27, 2008 | ||||
| Electronic Prescriptions for Controlled Substances | 36722–36782 [E8–14405] | Proposed Rule | Drug Enforcement Administration | |
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Part IV Department of Justice Drug Enforcement Administration 21 CFR Parts 1300, 1304, et al. Electronic Prescriptions for Controlled Substances; Proposed Rule DEPARTMENT OF
JUSTICE Drug Enforcement Administration 21 CFR Parts 1300, 1304, 1306 and 1311 [Docket No. DEA-218P] RIN 1117-AA61 Electronic Prescriptions for Controlled Substances AGENCY:
Drug Enforcement Administration (DEA), Department of Justice. ACTION: Notice of Proposed Rulemaking. SUMMARY: DEA is proposing to revise its... [read document] |
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| Controlled Substances Importer; Application | 36571–36572 [E8–14586] | Notice | Drug Enforcement Administration | |
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DEPARTMENT OF JUSTICE Drug Enforcement Administration Importer of Controlled Substances; Notice of Application Pursuant to 21 U.S.C. 958(i), the Attorney General shall, prior to
issuing a registration under this Section to a bulk manufacturer of a controlled substance in schedule I or II, and prior to issuing a registration under 21 U.S.C. 952(a)(2)
authorizing the importation of such substances, provide manufacturers holding registrations for the bulk manufacture of the substance an... [read document] |
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| Controlled Substances Importer; Registration | 36572–36573 [E8–14651] | Notice | Drug Enforcement Administration | |
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DEPARTMENT OF JUSTICE Drug Enforcement Administration Importer of Controlled Substances; Notice of Registration By Notice dated March 27, 2008 and published in the Federal
Register on April 2, 2008, (73 FR 18000), Stepan Company, Natural Products Department, 100 W. Hunter Avenue, Maywood, New Jersey 07607, made application by renewal to the Drug
Enforcement Administration (DEA) to be registered as an importer of Coca Leaves (9040), a basic class of controlled substance listed in schedule II.... [read document] |
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| Controlled Substances Importer; Registration | 36572 [E8–14584] | Notice | Drug Enforcement Administration | |
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DEPARTMENT OF JUSTICE Drug Enforcement Administration Importer of Controlled Substances; Notice of Registration By Notice dated March 19, 2008 and published in the Federal
Register on March 28, 2008, (73 FR 16718), Penick Corporation, 33 Industrial Park Road, Pennsville, New Jersey 08070, made application by renewal to the Drug Enforcement
Administration (DEA) to be registered as an importer of the basic classes of controlled substances listed in schedule II: Drug Schedule Coca Leaves (9040) II... [read document] |
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| Controlled Substances Importer; Application | 36572 [E8–14590] | Notice | Drug Enforcement Administration | |
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DEPARTMENT OF JUSTICE Drug Enforcement Administration Importer of Controlled Substances Notice of Application Pursuant to 21 U.S.C. 958(i), the Attorney General shall, prior to
issuing a registration under this Section to a bulk manufacturer of a controlled substance in schedule I or II, and prior to issuing a registration under 21 U.S.C. 952(a)(2)
authorizing the importation of such a substance, provide manufacturers holding registrations for the bulk manufacture of the substance an... [read document] |
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| Controlled Substances Manufacturer; Application | 36573 [E8–14588] | Notice | Drug Enforcement Administration | |
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DEPARTMENT OF JUSTICE Drug Enforcement Administration Manufacturer of Controlled Substances; Notice of Application Pursuant to Sec. 1301.33(a) of Title 21 of the Code of Federal
Regulations (CFR), this is notice that on May 7, 2008, Archimica, Inc., 2460 W. Bennett Street, Springfield, Missouri 65807-1229, made application by renewal to the Drug
Enforcement Administration (DEA) to be registered as a bulk manufacturer of the basic classes of controlled substances listed in schedule II: Drug... [read document] |
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| Controlled Substances Manufacturer; Application | 36573 [E8–14585] | Notice | Drug Enforcement Administration | |
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DEPARTMENT OF JUSTICE Drug Enforcement Administration Manufacturer of Controlled Substances; Notice of Application Pursuant to Sec. 1301.33(a) of Title 21 of the Code of Federal
Regulations (CFR), this is notice that on May 22, 2008, Norac Inc., 405 S. Motor Avenue, P.O. Box 577, Azusa, California 91702-3232, made application by letter to the Drug
Enforcement Administration (DEA) to be registered as a bulk manufacturer of Gamma Hydroxybutyric Acid (2010), a basic class of controlled substance... [read document] |
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| June 23, 2008 | ||||
| Proposed Revised Assessment of Annual Needs for the List I Chemicals: Ephedrine, Pseudoephedrine, and Phenylpropanolamine (for 2008) | 35410–35412 [E8–14108] | Notice | Drug Enforcement Administration | |
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DEPARTMENT OF JUSTICE Drug Enforcement Administration [Docket No. DEA-306R] Proposed Revised Assessment of Annual Needs for the List I Chemicals Ephedrine, Pseudoephedrine, and
Phenylpropanolamine for 2008 AGENCY: Drug Enforcement Administration (DEA), Justice. ACTION: Notice of proposed revised 2008 assessment of annual needs for the list I chemicals
ephedrine, pseudoephedrine, and phenylpropanolamine. SUMMARY: This notice proposes revised 2008 assessment of annual needs for the List I... [read document] |
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| June 20, 2008 | ||||
| Registration: Manufacturer of Controlled Substances | 35152–35153 [E8–13911] | Notice | Drug Enforcement Administration | |
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DEPARTMENT OF JUSTICE Drug Enforcement Administration Manufacturer of Controlled Substances; Notice of Registration By Notice dated February 20, 2008 and published in the
Federal Register on February 29, 2008, (73 FR 11149), Stepan Company, Natural Products Dept., 100 W. Hunter Avenue, Maywood, New Jersey 07607, made application by renewal to the
Drug Enforcement Administration (DEA) to be registered as a bulk manufacturer of the basic classes of controlled substances listed in schedule II:... [read document] |
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| Registration: Importer of Controlled Substances | 35152 [E8–13912] | Notice | Drug Enforcement Administration | |
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DEPARTMENT OF JUSTICE Drug Enforcement Administration Importer of Controlled Substances; Notice of Registration By Notice dated April 17, 2006 and published in the Federal
Register on April 21, 2006, (71 FR 20729), and as corrected by Notice dated May 15, 2006, and published in the Federal Register on May 22, 2006, (71 FR 29354), Rhodes
Technologies, 498 Washington Street, Coventry, Rhode Island 02816, made application to the Drug Enforcement Administration (DEA) to be registered as an importer... [read document] |
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| June 18, 2008 | ||||
| Revocation of Registration: Harriston Lee Bass, Jr., M.D | 34790–34791 [E8–13741] | Notice | Drug Enforcement Administration | |
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DEPARTMENT OF JUSTICE Drug Enforcement Administration [Docket No. 07-42] Harriston Lee Bass, Jr., M.D.; Revocation of Registration On June 18, 2007, the Deputy Assistant
Administrator, Office of Diversion Control, Drug Enforcement Administration, issued an Order to Show Cause to Harriston Lee Bass, M.D. (Respondent), of Las Vegas, Nevada. The
Show Cause Order proposed the revocation of Respondent's DEA Certificate of Registration, BB0816441, as a practitioner, and the denial of any pending... [read document] |
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| June 17, 2008 | ||||
| Application Denial: Craig H. Bammer, D.O | 34327–34329 [E8–13609] | Notice | Drug Enforcement Administration | |
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DEPARTMENT OF JUSTICE Drug Enforcement Administration Craig H. Bammer, D.O.; Denial of Application On October 1, 2007, the Deputy Assistant Administrator, Office of Diversion
Control, Drug Enforcement Administration, issued an Order to Show Cause to Craig H. Bammer, D.O. (Respondent), of South Gulfport, Florida. The Show Cause Order proposed the
revocation of Respondent's Certificate of Registration, BB1336456, as a practitioner, and the denial of any pending applications to renew or modify the... [read document] |
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| Application Denial: Benjamin Levine, M.D | 34329–34330 [E8–13617] | Notice | Drug Enforcement Administration | |
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DEPARTMENT OF JUSTICE Drug Enforcement Administration [Docket No. 07-52] Benjamin Levine, M.D.; Dismissal of Proceeding On August 7, 2007, the Deputy Assistant Administrator,
Office of Diversion Control, Drug Enforcement Administration, issued an Order to Show Cause to Benjamin Levine, M.D. (Respondent), of East Brunswick, New Jersey. The Show Cause
Order proposed the revocation of Respondent's DEA Certificate of Registration, BL3612480, as a practitioner, and the denial of any pending... [read document] |
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| Application Denial: William W. Nucklos, M.D | 34330 [E8–13618] | Notice | Drug Enforcement Administration | |
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DEPARTMENT OF JUSTICE Drug Enforcement Administration [Docket No. 07-40] William W. Nucklos, M.D.; Dismissal of Proceeding On June 18, 2007, the Deputy Assistant Administrator,
Office of Diversion Control, Drug Enforcement Administration, issued an Order to Show Cause to William W. Nucklos, M.D. (Respondent), of Powell, Ohio. The Show Cause Order
proposed the revocation of Respondent's registration, BN2037314, as a practitioner, and the denial of any pending application to renew his... [read document] |
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| June 10, 2008 | ||||
| Application; Importer of Controlled Substances: Cambrex Charles City, Inc | 32736 [E8–12983] | Notice | Drug Enforcement Administration | |
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DEPARTMENT OF JUSTICE Drug Enforcement Administration Importer of Controlled Substances; Notice of Application Pursuant to 21 U.S.C. 958(i), the Attorney General shall, prior to
issuing a registration under this Section to a bulk manufacturer of a controlled substance in schedule I or II, and prior to issuing a regulation under 21 U.S.C. 952(a)(2)(B)
authorizing the importation of such a substance, provide manufacturers holding registrations for the bulk manufacture of the substance an... [read document] |
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| June 6, 2008 | ||||
| Agency Information Collection Activities; Proposals, Submissions, and Approvals | 32359–32360 [E8–12703] | Notice | Drug Enforcement Administration | |
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DEPARTMENT OF JUSTICE Drug Enforcement Administration [OMB Number 1117-0023] Agency Information Collection Activities: Proposed Collection; Comments Requested ACTION: 60-Day
Notice of Information Collection Under Review; Import/ Export Declaration for List I and List II Chemicals--DEA Form 486. The Department of Justice (DOJ), Drug Enforcement
Administration (DEA), will be submitting the following information collection request to the Office of Management and Budget (OMB) for review and... [read document] |
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| June 2, 2008 | ||||
| Importer Of Controlled Substances; Registration: Lipomed, Inc | 31509–31510 [E8–12189] | Notice | Drug Enforcement Administration | |
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DEPARTMENT OF JUSTICE Drug Enforcement Administration Importer of Controlled Substances; Notice of Registration By Notice dated March 10, 2008 and published in the Federal
Register on March 19, 2008, (73 FR 14838), Lipomed, Inc., One Broadway, Cambridge, Massachusetts 02142, made application by renewal to the Drug Enforcement Administration (DEA)
to be registered as an importer of the basic classes of controlled substances listed in schedule I and II: Drug Schedule Cathinone (1235) I... [read document] |
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| Importer Of Controlled Substances; Registration: Kenco VPI | 31510 [E8–12190] | Notice | Drug Enforcement Administration | |
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DEPARTMENT OF JUSTICE Drug Enforcement Administration Importer of Controlled Substances; Notice of Registration By Notice dated March 11, 2008 and published in the Federal
Register on March 19, 2008, (73 FR 14840), Kenco VPI, Division of Kenco Group Inc., 350 Corporate Place, Chattanooga, Tennessee 37419, made application by renewal to the Drug
Enforcement Administration (DEA) to be registered as an importer of Nabilone (7379), a basic class of controlled substance listed in schedule II. The... [read document] |
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| May 28, 2008 | ||||
| Denial Of Application: Paul H. Volkman | 30630–30644 [E8–11851] | Notice | Drug Enforcement Administration | |
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DEPARTMENT OF JUSTICE Drug Enforcement Administration [No. 06-45] Paul H. Volkman; Denial of Application On February 10, 2006, I, the Deputy Administrator of the Drug
Enforcement Administration, issued an Order to Show Cause and Immediate Suspension of Registration to Paul H. Volkman, M.D. (Respondent), of Chillicothe, Ohio. The Order
immediately suspended Respondent's DEA Certificate of Registration, AV6952837, as a practitioner, on the grounds that his continued registration during the... [read document] |
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| May 27, 2008 | ||||
| Manufacturer of Controlled Substances Application: Siegfried (USA), Inc | 30418 [E8–11631] | Notice | Drug Enforcement Administration | |
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DEPARTMENT OF JUSTICE Drug Enforcement Administration Manufacturer of Controlled Substances; Notice of Application Pursuant to Sec. 1301.33(a) of Title 21 of the Code of Federal
Regulations (CFR), this is notice that on April 25, 2008, Siegfried (USA), Inc., Industrial Park Road, Pennsville, New Jersey 08070, made application by letter to the Drug
Enforcement Administration (DEA) to be registered as a bulk manufacturer of Oripavine(9330), a basic class of controlled substance listed in schedule... [read document] |
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| Manufacturer of Controlled Substances Application: AMRI Rensselaer, Inc | 30418–30419 [E8–11633] | Notice | Drug Enforcement Administration | |
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DEPARTMENT OF JUSTICE Drug Enforcement Administration Manufacturer of Controlled Substances; Notice of Application Pursuant to Sec. 1301.33(a) of Title 21 of the Code of Federal
Regulations (CFR), this is notice that on September 21, 2007, AMRI Rensselaer, Inc., 33 Riverside Avenue, Rensselaer, New York 12144, made application by renewal to the Drug
Enforcement Administration (DEA) as a bulk manufacturer of the basic classes of controlled substances listed in schedules I and II: Drug Schedule... [read document] |
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| May 22, 2008 | ||||
| Changes to Patient Limitation for Dispensing or Prescribing Approved Narcotic Controlled Substances for Maintenance or Detoxification Treatment by, etc | 29685–29688 [E8–11471] | Rule | Drug Enforcement Administration | |
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DEPARTMENT OF JUSTICE Drug Enforcement Administration 21 CFR Part 1301 [Docket No. DEA-275F] RIN 1117-AA99 Changes to Patient Limitation for Dispensing or Prescribing Approved
Narcotic Controlled Substances for Maintenance or Detoxification Treatment by Qualified Individual Practitioners AGENCY: Drug Enforcement Administration (DEA), Justice. ACTION:
Final rule. SUMMARY: On September 20, 2007, the Drug Enforcement Administration (DEA) published a Notice of Proposed Rulemaking (NPRM) in the... [read document] |
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| May 7, 2008 | ||||
| Agency Information Collection Activities; Proposals, Submissions, and Approvals | 25769–25770 [E8–10082] | Notice | Drug Enforcement Administration | |
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DEPARTMENT OF JUSTICE Drug Enforcement Administration [OMB Number 1117-0010] Agency Information Collection Activities ACTION: 30-day notice of information collection under
review. Proposed collection; comments requested: U.S. Official Order Forms for Schedule I and II Controlled Substances (Accountable Forms), Order Form Requisition--DEA Form 222
and 222a The Department of Justice (DOJ), Drug Enforcement Administration (DEA) will be submitting the following information collection request to the... [read document] |
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| Agency Information Collection Activities; Proposals, Submissions, and Approvals | 25770 [E8–10084] | Notice | Drug Enforcement Administration | |
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DEPARTMENT OF JUSTICE Drug Enforcement Administration [OMB Number 1117-0021] Agency Information Collection Activities: Proposed Collection; Comments Requested ACTION: 30-day
notice of information collection under review: Records and Reports of Registrants. The Department of Justice (DOJ), Drug Enforcement Administration (DEA) will be submitting the
following information collection request to the Office of Management and Budget (OMB) for review and approval in accordance with the Paperwork... [read document] |
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| May 2, 2008 | ||||
| Application: Manufacturer of Controlled Substances | 24313–24314 [E8–9694] | Notice | Drug Enforcement Administration | |
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DEPARTMENT OF JUSTICE Drug Enforcement Administration Manufacturer of Controlled Substances; Notice of Application Pursuant to Sec. 1301.33(a) of Title 21 of the Code of Federal
Regulations (CFR), this is notice that on April 2, 2008, Lin Zhi International Inc., 687 North Pastoria Avenue, Sunnyvale, California 94085, made application by renewal to the
Drug Enforcement Administration (DEA) to be registered as a bulk manufacturer of the basic classes of controlled substances listed in schedules I... [read document] |
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| Application: Abbott Laboratories | 24313 [E8–9696] | Notice | Drug Enforcement Administration | |
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DEPARTMENT OF JUSTICE Drug Enforcement Administration Manufacturer of Controlled Substances; Notice of Application Pursuant to Sec. 1301.33(a) of Title 21 of the Code of Federal
Regulations (CFR), this is notice that on April 3, 2008, Abbott Laboratories, DBA Knoll Pharmaceutical Company, 30 North Jefferson Road, Whippany, New Jersey 07981, made
application by renewal to the Drug Enforcement Administration (DEA) to be registered as a bulk manufacturer of the basic classes of controlled... [read document] |
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| Application: Importer of Controlled Substances | 24314–24315 [E8–9697] | Notice | Drug Enforcement Administration | |
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DEPARTMENT OF JUSTICE Drug Enforcement Administration Importer of Controlled Substances; Notice of Registration By Notice dated February 13, 2008 and published in the Federal
Register on February 21, 2008, (73 FR 9589), Sigma Aldrich Manufacturing LLC., 3500 Dekalb Street, St. Louis, Missouri 63118, made application to the Drug Enforcement
Administration (DEA) to be registered as an importer of the basic classes of controlled substances listed in schedule I and II: Drug Schedule Cathinone... [read document] |
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| April 25, 2008 | ||||
| Classification of Three Steroids as Schedule III Anabolic Steroids | 22294–22300 [E8–8842] | |||