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Contents (.PDF)   Federal Register

Contents (.TXT)                      Vol. 64, No.97

Thursday May 20, 1999

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Food and Drug Administration
NOTICES
Docket No. 98E-0840, OC99123. Determination of Regulatory Review Period for Purposes of Patent Extension; Omnicef Oral Suspension.  Pages 27579-27580 [FR Doc. 99-12654] [TXT]  [PDF]

Docket No. 98E-0754, OC99124.  Determination of Regulatory Review Period for Purposes of Patent Extension; Omnicef Tablets.  Page 27578 [FR Doc. 99-12651] [TXT]  [PDF]

Docket No. 98E-0474, OC99126. Determination of Regulatory Review Period for Purposes of Patent Extension; Tazorac.  Pages 27578-27579 [FR Doc. 99-12652] [TXT]  [PDF]

OC99134.  Blood Products Advisory Committee; Notice of Meeting.  Pages 27580-27581 [FR Doc. 99-12793] [TXT]  [PDF]

OC99132.   Circulatory Systems Devices Panel of the Medical Devices Advisory Committee; Notice of Meeting.  Page 27581 [FR Doc. 99-12792] [TXT]  [PDF]

OC99119.  Oncologic Drugs Advisory Committee; Notice of Meeting.  Pages 27581-27582 [FR Doc. 99-12852] [TXT]  [PDF]

OC99120.  Transmissible Spongiform Encephalopathies Advisory Committee; Notice of Meeting.  Page 27582 [FR Doc. 99-12653][TXT]  [PDF]

Docket No. 98D-1171, CBER9814.  Draft Guidance for Industry: For Platelet Testing and Evaluation of Platelet Substitute Products; Availability. Pages 27582-27583 [FR Doc. 99-12649] [TXT]  [PDF]  Written comments by July 19, 1999

The Guidance
Docket No. 97D-0528, CBER992.  Guidance for Industry: Efficacy Studies to Support Marketing of Fibrin Sealant Products Manufactured for Commercial Use; Availability.  Pages 27583-27584 [FR Doc. 99-12650][TXT]  [PDF]
The Guidance