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| Dockets Entered
On February 26, 2004
Table of Contents
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| Docket #
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| Title
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| 1978N-0021
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| Skin Protectant Drugs for OTC Human Use
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| 1978N-0021P
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| Skin Protectant Drug Products for OTC Human Use
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| 1995N-0304
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| Ephedrine Alkaloids: Reports of Adverse Events; Availability
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| 1996N-0417
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| CGMP in Mfg. Packing or Holding Dietary Supplements
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| 1997S-0162
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| 30-Day Structure Function Claim Notification Letters Dietary
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| 1998P-0151
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| Introduction Of Downed Cattle Into The Food Supply
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| 1999N-4282
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| Biotechnology in the Year 2000 and Beyond; Public Meetings
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| 1999P-1340
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| Declared Eternity eau de Parfum Misbranded
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| 2000P-1211
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| Establish Mandatory Pre-Market Safety Testing for GE Foods
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| 2001P-0239
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| ANDA Suitability for Amlodipine 'Caplet'
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| 2001P-0241
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| ANDA Suitability for Paroxetine 'Caplet'
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| 2002N-0204
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| Bar Code Label Requirements for human drug products
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| 2003D-0229
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| Draft Guidance for Industry on Continuous Marketing Applications: Pilot 2 - Scientific Feedback and Interactions During Development of Fast Track Products Under PDUFA
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| 2003D-0568
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| Guidance for Industry and FDA Staff; Class II Special Controls Guidance Document: Vascular and Neurovascular Embolization Devices
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| 2003H-0432
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| Civil Money Penalty, Korangy Radiology Associates, PA
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| 2003N-0198
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| Agency Information Collection Activities: Proposed Collection; Comment Request; Medicated Feed Mill License
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| 2003N-0567
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| Cardiovascular and Neurological Devices; Reclassification of Two Embolization Devices
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| 2004N-0062
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| Agency Information Collection Activities; Proposed Collection; Comment Request; Color Additive Certification Requests and Recordkeeping
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| 2004N-0077
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| Agency Emergency Processing Under OMB Review; Animal Drug User Fee Cover Sheet
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| 2004P-0091
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| To premarket approval (PMA) for the gastric electrical stimulation ( GES), level III device, enterra therapy, for the treatment of severe nausea and vomiting from gastroparesis
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| 1978N-0021
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| Skin Protectant Drugs for OTC Human Use
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| PAV
1
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| HFC-1 to The Cosmetic, Toiletry and Fragrance Association
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| Vol #:
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| 43
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| 1978N-0021P
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| Skin Protectant Drug Products for OTC Human Use
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| PAV
1
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| HFC-1 to The Cosmetic, Toiletry and Fragrance Association
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| Vol #:
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| 1
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| 1995N-0304
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| Ephedrine Alkaloids: Reports of Adverse Events; Availability
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| EMC 1246
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| Steve
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| Vol #:
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| 378
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| EMC 1247
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| M. Morris
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| Vol #:
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| 378
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| EMC 1248
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| B. Hernandez
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| Vol #:
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| 378
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| EMC 1249
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| J. Stacey
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| Vol #:
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| 378
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| EMC 1250
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| B. Peters
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| Vol #:
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| 378
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| EMC 1251
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| V. Courtney
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| Vol #:
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| 378
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| EMC 1252
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| A. Huey
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| Vol #:
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| 378
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| EMC 1253
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| No signature
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| Vol #:
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| 378
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| EMC 1254
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| T. Carr
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| Vol #:
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| 378
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| EMC 5785
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| Gordon Gacek
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| Vol #:
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| 789
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| EMC 5786
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| Tracey Smith
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| Vol #:
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| 789
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| 2001P-0239
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| ANDA Suitability for Amlodipine 'Caplet'
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| WDL
1
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| Cipher Pharmaceuticals Limited
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| Vol #:
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| 1
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| 2001P-0241
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| ANDA Suitability for Paroxetine 'Caplet'
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| WDL
1
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| Cipher Pharmaceuticals Limited
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| Vol #:
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| 1
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| 2002N-0204
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| Bar Code Label Requirements for human drug products
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| BKG 2
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| Refs 1 - 31 found in 69FR9120
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| Vol #:
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| 19
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| NFR
1
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| FDA
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| Vol #:
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| 19
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| 2003D-0229
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| Draft Guidance for Industry on Continuous Marketing Applications: Pilot 2 - Scientific Feedback and Interactions During Development of Fast Track Products Under PDUFA
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| N
3
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| FDA
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| Vol #:
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| 1
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| 2003D-0568
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| Guidance for Industry and FDA Staff; Class II Special Controls Guidance Document: Vascular and Neurovascular Embolization Devices
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| GDL
1
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| Guideline
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| Vol #:
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| 1
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| NAD
1
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| FDA
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| Vol #:
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| 1
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| 2003H-0432
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| Civil Money Penalty, Korangy Radiology Associates, PA
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| MO
4
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| GCF-1
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| Vol #:
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| 1
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| 2003N-0198
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| Agency Information Collection Activities: Proposed Collection; Comment Request; Medicated Feed Mill License
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| SS
1
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| Supporting Statement
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| Vol #:
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| 1
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| 2003N-0567
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| Cardiovascular and Neurological Devices; Reclassification of Two Embolization Devices
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| NPR
1
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| FDA
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| Vol #:
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| 1
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| 2004N-0062
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| Agency Information Collection Activities; Proposed Collection; Comment Request; Color Additive Certification Requests and Recordkeeping
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| N
1
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| FDA
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| Vol #:
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| 1
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| 2004N-0077
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| Agency Emergency Processing Under OMB Review; Animal Drug User Fee Cover Sheet
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| N
1
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| FDA
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| Vol #:
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| 1
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| 2004P-0091
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| To premarket approval (PMA) for the gastric electrical stimulation ( GES), level III device, enterra therapy, for the treatment of severe nausea and vomiting from gastroparesis
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| ACK
1
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| HFA-305 to Gastroparcsis & Dysmotilities Assn.
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| Vol #:
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| 1
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| CP
1
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| Gastroparcsis & Dysmotilities Assn.
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| Vol #:
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| 1
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