Documents
Briefs, oral arguments, agency decisions and the Federal Register.
9,603 results
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Final Results of Antidumping Duty Administrative Reviews: Electrolytic Manganese Dioxide From Japan
Federal Register · Uncategorized Document · Oct 21, 1994
TOSOH did not comment on either the 1991-1992 review or the 1992-1993 review. … The Department has completed these reviews in accordance with section 751 of the Tariff Act of 1930, as amended (the Act).
Commerce DepartmentInternational Trade AdministrationDetermination of Regulatory Review Period for Purposes of Patent Extension; MycobutinSUPTM
Federal Register · Uncategorized Document · Apr 15, 1994
Under these acts, a product's regulatory review period forms the basis for determining the amount of extension an applicant may receive. … These periods of time were derived from the following dates: 1. The date an exemption under section 505(i) of the Federal Food, Drug, and Cosmetic Act became effective: March 23, 1986.
Health and Human Services DepartmentFood and Drug AdministrationDetermination of Regulatory Review Period for Purposes of Patent Extension; ZeritRegister
Federal Register · Uncategorized Document · Nov 16, 1994
Under these acts, a product's regulatory review period forms the basis for determining the amount of extension an applicant may receive. … These periods of time were derived from the following dates: 1. The date an exemption under section 505(i) of the Federal Food, Drug, and Cosmetic Act became effective: January 19, 1989.
Health and Human Services DepartmentDetermination of Regulatory Review Period for Purposes of Patent Extension; NeutrexinSUPTM
Federal Register · Uncategorized Document · Aug 30, 1994
Under these acts, a product's regulatory review period forms the basis for determining the amount of extension an applicant may receive. … These periods of time were derived from the following dates: 1. The date an exemption under section 505(i) of the Federal Food, Drug, and Cosmetic Act became effective: October 21, 1987.
Health and Human Services DepartmentDetermination of Regulatory Review Period for Purposes of Patent Extension; KytrilSUPTM
Federal Register · Uncategorized Document · Aug 30, 1994
Under these acts, a product's regulatory review period forms the basis for determining the amount of extension an applicant may receive. … These periods of time were derived from the following dates: 1. The date an exemption under section 505(i) of the Federal Food, Drug, and Cosmetic Act became effective: July 14, 1988.
Health and Human Services DepartmentDetermination of Regulatory Review Period for Purposes of Patent Extension; LipidilRegister
Federal Register · Uncategorized Document · Aug 30, 1994
Under these acts, a product's regulatory review period forms the basis for determining the amount of extension an applicant may receive. … These periods of time were derived from the following dates: 1. The date an exemption under section 505(i) of the Federal Food, Drug, and Cosmetic Act became effective: September 6, 1981.
Health and Human Services DepartmentDetermination of Regulatory Review Period for Purposes of Patent Extension; ZosynRegister
Federal Register · Uncategorized Document · Aug 30, 1994
Under these acts, a product's regulatory review period forms the basis for determining the amount of extension an applicant may receive. … These periods of time were derived from the following dates: 1. The date an exemption under section 505(i) of the Federal Food, Drug, and Cosmetic Act became effective: October 31, 1988.
Health and Human Services DepartmentDetermination of Regulatory Review Period for Purposes of Patent Extension; EffexorRegister
Federal Register · Uncategorized Document · Aug 30, 1994
Under these acts, a product's regulatory review period forms the basis for determining the amount of extension an applicant may receive. … These periods of time were derived from the following dates: 1. The date an exemption under section 505(i) of the Federal Food, Drug, and Cosmetic Act became effective: November 23, 1985.
Health and Human Services DepartmentDetermination of Regulatory Review Period for Purposes of Patent Extension; DemadexSUPTM
Federal Register · Uncategorized Document · Jul 21, 1994
Under these acts, a product's regulatory review period forms the basis for determining the amount of extension an applicant may receive. … These periods of time were derived from the following dates: 1. The date an exemption under section 505(i) of the Federal Food, Drug, and Cosmetic Act became effective: January 4, 1986.
Health and Human Services DepartmentIndustrial Phosphoric Acid From Israel; Final Results of Antidumping Duty Administrative Reviews
Federal Register · Uncategorized Document · Jun 22, 1994
The Department has now completed these administrative reviews in accordance with section 751 of the Tariff Act of 1930, as amended (the Act). … Analysis of Comments Received We gave interested parties an opportunity to comment on the preliminary results. We received no comments.
Commerce DepartmentFederal Register · Uncategorized Document · Jul 22, 1999
These changes included new legislation such as the Personal Responsibility and Work Opportunity Reconciliation Act, the Work Incentives Improvement Act, and the Workforce Investment Act. … However, there is insufficient time to allow for a complete SPOC comment period. Therefore, we have reduced the comment period to 30 days from the closing date for applications.
64 FR 39860Health and Human Services DepartmentChildren and Families AdministrationTomatoes Grown in Florida; Expenses and Assessment Rate
Federal Register · Uncategorized Document · Nov 3, 1994
Comments received by December 5, 1994, will be considered prior to issuance of a final rule. ADDRESSES: Interested persons are invited to submit written comments concerning this action. … period, and all comments timely received will be considered prior to finalization of this action.
Agriculture DepartmentFederal Register · Uncategorized Document · Mar 22, 1994
This hearing and reopened comment period will allow comments on this proposal to be submitted from all interested parties. … a public hearing during the original comment period.
Interior DepartmentFish and Wildlife ServiceFederal Register · Uncategorized Document · Sep 1, 1994
In addressing this issue, commenters are encouraged to address whether core provisions in consumer protection orders ordinarily will have served their remedial purposes within a specified time period, … The Administrative Procedure Act permits the Commission to amend its rules in this fashion without a public comment period. 5 U.S.C.
Federal Trade CommissionIdaho-Eastern Oregon Onions; Expenses and Assessment Rate
Federal Register · Uncategorized Document · May 12, 1994
Comments received by June 13, 1994 will be considered prior to issuance of a final rule. ADDRESSES: Interested persons are invited to submit written comments concerning this action. … action which was unanimously recommended by the Committee at a public meeting and is similar to other budget actions issued in past years; and (4) this interim final rule provides a 30-day comment period
Agriculture DepartmentAgricultural Marketing ServiceDetermination of Regulatory Review Period for Purposes of Patent Extension; SemprexSUPTM-D Capsules
Federal Register · Uncategorized Document · Sep 21, 1994
Under these acts, a product's regulatory review period forms the basis for determining the amount of extension an applicant may receive. … These periods of time were derived from the following dates: 1. The date an exemption under section 505(i) of the Federal Food, Drug, and Cosmetic Act became effective: September 6, 1984.
Health and Human Services DepartmentFood and Drug AdministrationDetermination of Regulatory Review Period for Purposes of Patent Extension; DovonexRegister
Federal Register · Uncategorized Document · Aug 29, 1994
Under these acts, a product's regulatory review period forms the basis for determining the amount of extension an applicant may receive. … These periods of time were derived from the following dates: 1. The date an exemption under section 505(i) of the Federal Food, Drug, and Cosmetic Act became effective: November 8, 1990.
Health and Human Services DepartmentDetermination of Regulatory Review Period for Purposes of Patent Extension; LivostinRegister
Federal Register · Uncategorized Document · Aug 30, 1994
Under these acts, a product's regulatory review period forms the basis for determining the amount of extension an applicant may receive. … These periods of time were derived from the following dates: 1. The date an exemption under section 505(i) of the Federal Food, Drug, and Cosmetic Act became effective: April 4, 1986.
Health and Human Services DepartmentRunaway and Homeless Youth Program Proposed Priorities for Fiscal Year 1994
Federal Register · Uncategorized Document · Jan 28, 1994
period ends. … period ends.
Health and Human Services DepartmentFederal Register · Uncategorized Document · Aug 30, 1994
The OTS solicited public comments on all aspects of the proposal for a 30-day period. … The OTS has carefully considered all of the comments received during the comment period.
Treasury DepartmentThrift Supervision Office
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