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Dockets Management

Dockets Entered On August 16, 2007
Docket # Title
1997S-0162 30-Day Structure Function Claim Notification Letters Dietary
2005D-0112 Guidance for Industry on Clinical Trial Endpoints for the Approval of Cancer Drugs and Biologics
2005D-0348 Guidance for Industry and Food and Drug Administration: Procedures for Handling Post-Approval Studies Imposed by PMA Order
2005N-0272 Irradiation in the Production, Processing & Handling of Food
2006D-0079 Guidance for Industry: Guide to Minimize Food Safety Hazards for Fresh-cut Fruits and Vegetables
2006D-0347 Guidance for Industry, Clinical Laboratories, and FDA Staff on In Vitro Diagnostic Multivariate Index Assays
2006N-0104 Agency Information Collection Activities: Proposed Collection; Comment Request; Requirements for Submission of Labeling for Human Prescription Drugs and Biologics in Electronic Format
2006N-0454 Use of Ozone-Depleting Substances; Removal of Essential-Use Designations
2007D-0025 Guidance for Industry: Class II Special Controls Guidance Document: Cord Blood Processing System and Storage Container; Availability
2007D-0117 Guidance for Industry on Orally Disintegrating Tablets
2007D-0168 Draft Guidances for Industry Describing Product-Specific Bioequivalence Recommendations
2007D-0185 Guidance for Industry and Review Staff on Labeling for Human Prescription Drugs Determining Established Pharmacologic Class for Use in the Highlights of Prescribing Information
2007D-0201 Guidance for Industry and Food and Drug Administration Staff; Premarket Notification (510(k)) Submissions for Medical Devices That Include Antimicrobial Agents
2007D-0249 Guidance for Industry: Preparation of IDEs and INDs for Products Intended to Repair or Replace Knee Cartilage
2007D-0268 Guidance for Industry and Food and Drug Administration Staff; Class II Special Controls Guidance Document: Absorbable Poly(hydroxybutyrate) Surgical Suture Produced by Recombinant DNA Technology
2007M-0161 Premarket Approval for AxSYM AUSAB by Abbott Laboratories, P060003
2007N-0064 Electronic Case Report Form Submission; Notice of Pilot Project
2007N-0073 Agency Information Collection Activities; Proposed Collection; Comment Request; Control of Communicable Diseases; Restrictions on African Rodents, Prairie Dogs, and Certain Other Animals
2007N-0198 Medical Devices; General Hospital and Personal Use Devices; Classification of the Filtering facepiece respirator for use by the general public in public health medical emergencies
2007N-0264 Revisions to the Requirements Applicable to Blood, Blood Components and Source Plasma, Direct Final Rule
2007N-0277 Food Labeling: Use of Symbols to Communicate Nutrition Information, Consideration of Consumer Studies and Nutritional Criteria; Public Hearing
2007N-0305 Current Good Manufacturing Practice Regulations for Medicated Feeds; Agency Information Collection Activities
2007N-0306 Current Good Manufacturing Practice Regulations for Type A Medicated Articles; Agency Information Collection Activities
2007P-0070 Make fluoride a prescription drug for use in tooth application, tooth paste, and in bottled water
2007P-0074 Take specific action with respect to 21 CFR 341, the Final Monograph for Cough, Cold Allergy, Bronchodilator, Antiasthmatic Drug Products for Over-the-Counter Human Use
2007P-0282 Require all products labels to include this information: Products % Costs Packaging: 80% Content: 20%
1997S-0162 30-Day Structure Function Claim Notification Letters Dietary
LET 20527 Aboca USA Inc. Vol #: 180
LET 20528 Aboca USA Inc. Vol #: 180
LET 20529 Aboca USA Inc. Vol #: 180
LET 20530 Aboca USA Inc. Vol #: 180
LET 20531 Aboca USA Inc. Vol #: 180
LET 20532 Aboca USA Inc. Vol #: 180
LET 20533 Aboca USA Inc. Vol #: 180
LET 20534 Nexgen Pharma tm, Inc. Vol #: 180
LET 20535 Nexgen Pharma tm, Inc. Vol #: 180
LET 20536 Sante' Active Vol #: 180
LET 20537 Bayer HealthCare LLC Consumer Care Division Vol #: 180
LET 20538 Bayer HealthCare LLC Consumer Care Division Vol #: 180
LET 20539 Enzymatic Therapy, Inc. Vol #: 180
LET 20540 Enzymatic Therapy, Inc. Vol #: 180
2005D-0112 Guidance for Industry on Clinical Trial Endpoints for the Approval of Cancer Drugs and Biologics
EC 43 ND. Doctors Protest of new durgs Vol #: 1
2005D-0348 Guidance for Industry and Food and Drug Administration: Procedures for Handling Post-Approval Studies Imposed by PMA Order
EC 5 Mr. Franklin Taylor Vol #: 1
2005N-0272 Irradiation in the Production, Processing & Handling of Food
C 3745 Form Letter Count 6 Vol #: 62
2006D-0079 Guidance for Industry: Guide to Minimize Food Safety Hazards for Fresh-cut Fruits and Vegetables
EC 47 private citizen Vol #: 1
2006D-0347 Guidance for Industry, Clinical Laboratories, and FDA Staff on In Vitro Diagnostic Multivariate Index Assays
EC 90 Biotechnology Industry Organization Vol #: 2
EC 91 Washington University School of Medicine Vol #: 2
2006N-0104 Agency Information Collection Activities: Proposed Collection; Comment Request; Requirements for Submission of Labeling for Human Prescription Drugs and Biologics in Electronic Format
EC 4 Surgical Migraine Clinic Vol #: 1
EC 5 Laboratorios Feltrex Vol #: 1
EC 6 Mr. :Ronald :Schulz Vol #: 1
2006N-0454 Use of Ozone-Depleting Substances; Removal of Essential-Use Designations
EC 20 American Society of Health-System Pharmacists Vol #: 1
EC 21 Academy of Managed Care Pharmacy Vol #: 1
EC 22 Cystic Fibrosis Foundation Vol #: 1
EC 23 Henry Ford Health System Vol #: 1
EC 24 Mr. Robert McClearen Vol #: 1
EC 25 Ms. Eva Herr Vol #: 1
EC 26 Mr. James Weaver Vol #: 1
EC 27 The National Orhanization Of Asthma And COPD Patie Vol #: 1
2007D-0025 Guidance for Industry: Class II Special Controls Guidance Document: Cord Blood Processing System and Storage Container; Availability
EC 3 HemoGenix, Inc Vol #: 2
EC 4 Ms. Sandra Nelson Vol #: 2
2007D-0117 Guidance for Industry on Orally Disintegrating Tablets
C 12 Catalent Vol #: 1
2007D-0168 Draft Guidances for Industry Describing Product-Specific Bioequivalence Recommendations
EC 1 Surgical migraine clinic Vol #: 1
2007D-0185 Guidance for Industry and Review Staff on Labeling for Human Prescription Drugs Determining Established Pharmacologic Class for Use in the Highlights of Prescribing Information
EC 1 GlaxoSmithKline Vol #: 1
EC 2 Pharm Res Vol #: 1
EC 3 Dr. Richard Gural Vol #: 1
EC 4 Eli Lilly and Company Vol #: 1
EC 5 Merck Research Laboratories Vol #: 1
EC 6 Genzyme Corp. Vol #: 1
2007D-0201 Guidance for Industry and Food and Drug Administration Staff; Premarket Notification (510(k)) Submissions for Medical Devices That Include Antimicrobial Agents
EC 1 Surgical migraine clinic Vol #: 1
2007D-0249 Guidance for Industry: Preparation of IDEs and INDs for Products Intended to Repair or Replace Knee Cartilage
EC 2 private citizen Vol #: 1
2007D-0268 Guidance for Industry and Food and Drug Administration Staff; Class II Special Controls Guidance Document: Absorbable Poly(hydroxybutyrate) Surgical Suture Produced by Recombinant DNA Technology
EC 2 Mrs. barbara white Vol #: 1
EC 3 Ms. Marjorie Moss Vol #: 1
2007M-0161 Premarket Approval for AxSYM AUSAB by Abbott Laboratories, P060003
AAV 1 Abbott Laboratories Vol #: 1
2007N-0064 Electronic Case Report Form Submission; Notice of Pilot Project
EC 1 Raining Data Vol #: 1
2007N-0073 Agency Information Collection Activities; Proposed Collection; Comment Request; Control of Communicable Diseases; Restrictions on African Rodents, Prairie Dogs, and Certain Other Animals
N 2 FDA Vol #: 1
2007N-0198 Medical Devices; General Hospital and Personal Use Devices; Classification of the Filtering facepiece respirator for use by the general public in public health medical emergencies
BKG 1 Background Vol #: 1
NFR 1 FDA Vol #: 1
2007N-0264 Revisions to the Requirements Applicable to Blood, Blood Components and Source Plasma, Direct Final Rule
NFR 1 FDA Vol #: 1
NPR 1 FDA Vol #: 1
2007N-0277 Food Labeling: Use of Symbols to Communicate Nutrition Information, Consideration of Consumer Studies and Nutritional Criteria; Public Hearing
EC 4 Mr. CAZIER OBERHANSLY Vol #: 1
2007N-0305 Current Good Manufacturing Practice Regulations for Medicated Feeds; Agency Information Collection Activities
N 1 FDA Vol #: 1
2007N-0306 Current Good Manufacturing Practice Regulations for Type A Medicated Articles; Agency Information Collection Activities
N 1 FDA Vol #: 1
2007P-0070 Make fluoride a prescription drug for use in tooth application, tooth paste, and in bottled water
EC 47 Mrs. Brenda Moore Vol #: 1
EC 48 Mrs. christine tabrizi Vol #: 1
EC 49 private citizen Vol #: 1
EC 50 Ms. Kristi Gabriel Vol #: 1
2007P-0074 Take specific action with respect to 21 CFR 341, the Final Monograph for Cough, Cold Allergy, Bronchodilator, Antiasthmatic Drug Products for Over-the-Counter Human Use
NM 1 FDA Vol #: 1
2007P-0282 Require all products labels to include this information: Products % Costs Packaging: 80% Content: 20%
EC 4 UVM GIV Camp Vol #: 1

Page created on August 16, 2007 ue

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