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| Dockets Entered
On December 14, 2007
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| Docket
#
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| Title
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| 2006F-0409
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| Safe Use of Cetylpyridinium Chloride as an Antimicrobial Agent in a Pre-chiller or Post-chiller Solution for Application to Raw Poultry Carcasses (FAP 6A4767)
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| 2006N-0168
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| Food Labeling: Reference Daily Intakes & Daily Reference Values
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| 2006N-0221
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| Requirements for Human Blood and Blood Components Intended for Transfusion or for Further Manufacturing Use
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| 2007D-0386
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| Guidance for Industry on Postmarketing Adverse Event Reporting for Nonprescription Human Drug Products Marketed Without an Approved Application
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| 2007D-0387
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| GIn Vitro Diagnostic Device Studies Frequently Asked Questions;Guidance for Industry and FDA Staff
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| 2007D-0388
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| Guidance for Industry: Questions and Answers Regarding Adverse Event Reporting and Recordkeeping for Dietary Supplements as Required by the Dietary Supplement and Nonprescription Drug Consumer Protec
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| 2007D-0396
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| Drug-Induced Liver Injury: Premarketing Clinical Evaluation;Draft Guidance
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| 2007N-0280
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| Amendment to the CGMP Regulations for Finished Pharmaceuticals
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| 2007N-0356
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| BEHIND THE COUNTER AVAILABILITY OF CERTAIN DRUGS; Public Meeting
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| 2007P-0438
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| Declare Angel Parfum, Angel Eau du Toilette and other Angel related fragranced products be declared misbranded and have their importation ceased until their safety can be independently verified
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| 2006F-0409
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| Safe Use of Cetylpyridinium Chloride as an Antimicrobial Agent in a Pre-chiller or Post-chiller Solution for Application to Raw Poultry Carcasses (FAP 6A4767)
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| EC 9
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| Miss. erin young
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| Vol #:
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| 1
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| 2006N-0168
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| Food Labeling: Reference Daily Intakes & Daily Reference Values
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| EXT 4
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| Food Products Association
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| Vol #:
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| 1
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| 2006N-0221
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| Requirements for Human Blood and Blood Components Intended for Transfusion or for Further Manufacturing Use
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| EC 7
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| PPTA
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| Vol #:
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| 1
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| EC 8
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| Puget Sound Blood Center
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| Vol #:
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| 1
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| 2007D-0386
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| Guidance for Industry on Postmarketing Adverse Event Reporting for Nonprescription Human Drug Products Marketed Without an Approved Application
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| C 1
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| Johnson & Johnson
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| Vol #:
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| 1
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| C 2
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| American Herbal Products Association
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| Vol #:
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| 1
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| 2007D-0387
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| GIn Vitro Diagnostic Device Studies Frequently Asked Questions;Guidance for Industry and FDA Staff
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| C 1
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| Eli Lilly and Company
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| Vol #:
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| 1
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| 2007D-0388
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| Guidance for Industry: Questions and Answers Regarding Adverse Event Reporting and Recordkeeping for Dietary Supplements as Required by the Dietary Supplement and Nonprescription Drug Consumer Protec
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| C 1
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| American Herbal Products Association
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| Vol #:
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| 1
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| EC 2
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| Natural Products Association
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| Vol #:
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| 1
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| EC 3
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| Center for Science in the Public Interest
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| Vol #:
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| 1
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| EC 4
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| CHPA
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| Vol #:
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| 1
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| 2007D-0396
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| Drug-Induced Liver Injury: Premarketing Clinical Evaluation;Draft Guidance
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| EC 1
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| AstraZeneca LP
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| Vol #:
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| 1
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| 2007N-0280
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| Amendment to the CGMP Regulations for Finished Pharmaceuticals
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