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Dockets Management
Dockets Entered On July 6, 2005
Table of Contents
Docket # Title
1975N-0256 Food Labeling & Label Declaration of Ingredient Requireme
1996P-0230 Grant exception for label declaration of ingredients/b olive
1998P-0151 Introduction Of Downed Cattle Into The Food Supply
2004D-0333 Emergency Use Authorization of Medical Products
2004N-0432 Radioactive Drugs for Certain Research Uses; Public Meeting
2004N-0463 Food Labeling: Prominence of Calories
2004N-0539 Establishing a Docket for the Development of Plasma Standards Public Workshop; Availability
2004P-0353 ANDA Suitability for Famotidine Orally Dissolving Strips 10 mg
2004P-0373 ANDA for Omeprazole Magnesium Delayed Release Capsules,Eq. to 20 mg base for OTC
2005N-0157 Agency Information Collection Activities: Proposed Collection; Postmarketing Adverse Drug Experience Reporting
1975N-0256 Food Labeling & Label Declaration of Ingredient Requireme
C 508 Mrs. Thomas J. Curran Vol #: 1
1996P-0230 Grant exception for label declaration of ingredients/b olive
LET 2 HFS-822 to Hyman, Phelps & McNamara, P.C. Vol #: 1
1998P-0151 Introduction Of Downed Cattle Into The Food Supply
C 7492 J. Kahl Vol #: 319
2004D-0333 Emergency Use Authorization of Medical Products
NAD 1 FDA Vol #: 1
2004N-0432 Radioactive Drugs for Certain Research Uses; Public Meeting
C 7 Harvard Medical School Vol #: 2
C 8 S. Kaste, DO Vol #: 2
2004N-0463 Food Labeling: Prominence of Calories
C 46 F. Levin Vol #: 4
C 47 AARP Vol #: 4
2004N-0539 Establishing a Docket for the Development of Plasma Standards Public Workshop; Availability
C 2 Plasma Protein Therapeutics Assn (PPTA) Vol #: 1
C 3 European Pharmacopoeia (EU) Vol #: 1
2004P-0353 ANDA Suitability for Famotidine Orally Dissolving Strips 10 mg
PAV 1 HFD-600 to Lachman Consultant Services, Inc. Vol #: 1
2004P-0373 ANDA for Omeprazole Magnesium Delayed Release Capsules,Eq. to 20 mg base for OTC
PAV 1 HFD-600 to Gray Cary Ware & Freidenrich LLP Vol #: 1
2005N-0157 Agency Information Collection Activities: Proposed Collection; Postmarketing Adverse Drug Experience Reporting
C 1 Wyeth Pharmaceuticals (Wyeth) Vol #: 1

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