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Dockets Management

Dockets Entered On December 12, 2007
Docket # Title
1978N-0038 Sunscreen Drug Products
2006N-0454 Use of Ozone-Depleting Substances; Removal of Essential-Use Designations
2006P-0394 Revise the labeling requirements for eggs sold in the United States
2007D-0310 Companion to Guidance for Industry on Pharmacogenomic Data
2007D-0364 Impact-Resistant Lenses: Questions and Answers Guidance
2007D-0365 Guidance for Industry on The Use of Mechanical Calibration of Dissolution Apparatus 1 and 2 Current Good Manufacturing Practice (CGMP)
2007D-0387 GIn Vitro Diagnostic Device Studies Frequently Asked Questions;Guidance for Industry and FDA Staff
2007N-0356 BEHIND THE COUNTER AVAILABILITY OF CERTAIN DRUGS; Public Meeting
2007N-0472 Agency Emergency Processing Under OMB Review; Certification to Accompany Drug, Biological Product, and Device Applications or Submissions
2007P-0085 Adopt Regulations of General Applicability to all Food Standards that would Permit Deviations from the Requirements of the Individual Food Standards of Identity
2007V-0476 Laser Display Device
2007V-0477 Laser Light Show
1978N-0038 Sunscreen Drug Products
EREG 17 BASF Aktiengesellschaft Vol #: 170
2006N-0454 Use of Ozone-Depleting Substances; Removal of Essential-Use Designations
C 4265 L. Shimmings Vol #: 40
C 4266 M. Yow Vol #: 40
C 4267 S. Wilhelm Vol #: 40
C 4268 J. Miller Vol #: 40
C 4269 N. Thomas Vol #: 40
C 4270 C. Maldonado Vol #: 40
2006P-0394 Revise the labeling requirements for eggs sold in the United States
C 507 A. Hacker Vol #: 14
C 508 R. Palumbo Vol #: 14
C 509 A. Ford Vol #: 14
2007D-0310 Companion to Guidance for Industry on Pharmacogenomic Data
EMC 1 Japan Pharmaceutical Manufacturers Association (JPMA) Vol #: 1
2007D-0364 Impact-Resistant Lenses: Questions and Answers Guidance
EC 8 emory university Vol #: 1
EC 9 Rutland Optical, Inc Vol #: 1
EC 10 Mr. gary stephens Vol #: 1
EC 11 Personal Eyes Vol #: 1
EC 12 Mr. Joe Brown Vol #: 1
2007D-0365 Guidance for Industry on The Use of Mechanical Calibration of Dissolution Apparatus 1 and 2 Current Good Manufacturing Practice (CGMP)
EC 2 Takao Manufacturing Co., Ltd. Vol #: 1
2007D-0387 GIn Vitro Diagnostic Device Studies Frequently Asked Questions;Guidance for Industry and FDA Staff
EC 1 Eli Lilly and Company Vol #: 1
2007N-0356 BEHIND THE COUNTER AVAILABILITY OF CERTAIN DRUGS; Public Meeting
C 6 T. P. Stone Vol #: 2
2007N-0472 Agency Emergency Processing Under OMB Review; Certification to Accompany Drug, Biological Product, and Device Applications or Submissions
N 1 FDA Vol #: 1
2007P-0085 Adopt Regulations of General Applicability to all Food Standards that would Permit Deviations from the Requirements of the Individual Food Standards of Identity
C 361 D. White Vol #: 102
2007V-0476 Laser Display Device
ACK 1 FDA/ DDM/ to X- Laser, L. L. C. Vol #: 1
VAR 1 X- Laser, L. L. C. Vol #: 1
2007V-0477 Laser Light Show
ACK 1 FDA/ DDM/ to X- Laser L. L. C. Vol #: 1
VAR 1 X- Laser L. L. C. Vol #: 1

Page created on December 12, 2007 ue

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