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Contents (.PDF)              Federal Register

Contents (.TXT)              Vol. 64, No.18

Thursday, January 28, 1999

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Food and Drug Administration
RULES
Docket No. 95N-0313, CVM97156. Standards for Animal Food and Food Additives in Standardized Animal Food. Pages  4293-4294 [FR Doc. 99-2057] [TXT] [PDF]
NOTICES
Docket No. 98E-0616, OC9919. Determination of Regulatory Review Period for Purposes of Patent Extension; Prandin (5,216,167).  Pages  4425-4426 [FR Doc. 99-1936] [TXT] [PDF]  Written comments by  March 29, 1999 and petitions by July 27, 1999.

Docket No. 98E-0475, OC9920. Determination of Regulatory Review Period for Purposes of Patent Extension; Prandin (5,312,9240).  Page 4426 [FR Doc. 99-1937  [TXT] [PDF] Written comments by  March 29, 1999 and petitions by July 27, 1999.

Docket No. 99N-0053, OC9912. Announcement of a Pilot Customer Satisfaction Survey: Medical Device Inspection Evaluation.  Pages 4426-4431 [FR Doc. 99-2014]   [TXT] [PDF] Written comments between March 1, 1999 through February 28, 2000.

Docket No. 98N-0148, OC9923. Open Meeting on World Health Organization Recommendations on Ephedrine and Other Substances.  Page 4432 [FR Doc. 99-2058]  [TXT] [PDF]

Docket No. 98D-0075, CDER98193. Guidance for Industry on General Considerations for Providing Regulatory Submissions in Electronic Format; Availability.  Pages  4433-4434 [FR Doc. 99-2059] [TXT] [PDF]

THE GUIDANCE
Docket No. 99D-0054, CDER997. Guidance for Industry on Providing Regulatory Submissions in Electronic Format--NDA's; Availability.  Pages 4432-4433 [FR Doc. 99-2060]  [TXT] [PDF]
THE GUIDANCE
Docket No. 98D-1266, CDER98108. Draft Guidance for Industry on Placing the Therapeutic Equivalence Code on Prescription Drug Labels and Labeling; Availability.  Pages  4434-4435 [FR Doc. 99-2015] [TXT] [PDF]
THE GUIDANCE