Code of Federal Regulations: Containing a Codification of Documents of General Applicability and Future Effect as of December 31, 1948, with Ancillaries and IndexDivision of the Federal Register, the National Archives, 2000 Special edition of the Federal Register, containing a codification of documents of general applicability and future effect ... with ancillaries. |
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Side vii
... submitted for publication in accordance with 1 CFR part 51 . law Properly approved incorporations by reference in this volume are listed in the Finding Aids at the end of this volume . What if the material incorporated by reference ...
... submitted for publication in accordance with 1 CFR part 51 . law Properly approved incorporations by reference in this volume are listed in the Finding Aids at the end of this volume . What if the material incorporated by reference ...
Side 12
... submitted at or prior to the hearing , the district director shall specify a time limit , reasonable in the light of the circumstances , for filing such application . §1.95 Application for authorization to relabel and recondition . to ...
... submitted at or prior to the hearing , the district director shall specify a time limit , reasonable in the light of the circumstances , for filing such application . §1.95 Application for authorization to relabel and recondition . to ...
Side 19
... submitted for the following products included in the classes of products listed in paragraph ( e ) of this section : ( i ) Ergotamine tartrate supplied in a metered - dose aerosol form suitable for oral inhalation for the treatment of ...
... submitted for the following products included in the classes of products listed in paragraph ( e ) of this section : ( i ) Ergotamine tartrate supplied in a metered - dose aerosol form suitable for oral inhalation for the treatment of ...
Side 39
... submitted under § 10.30 of this chapter for a stay of an effective date in $ 201.59 of this chapter for compli- ance with certain labeling require- ments for human prescription drugs . ( 1 ) ( i ) The Director and Deputy Direc- tor ...
... submitted under § 10.30 of this chapter for a stay of an effective date in $ 201.59 of this chapter for compli- ance with certain labeling require- ments for human prescription drugs . ( 1 ) ( i ) The Director and Deputy Direc- tor ...
Side 40
... submitted under §10.30 of this chapter requesting exemption from the general pregnancy - nursing warning for over- the - counter ( OTC ) drugs required under $ 201.63 of this chapter , requesting ex- emption from a general overdose warn ...
... submitted under §10.30 of this chapter requesting exemption from the general pregnancy - nursing warning for over- the - counter ( OTC ) drugs required under $ 201.63 of this chapter , requesting ex- emption from a general overdose warn ...
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Code of Federal Regulations: Containing a Codification of Documents of ... Uten tilgangsbegrensning - 1976 |
Code of Federal Regulations: Containing a Codification of Documents of ... Uten tilgangsbegrensning - 1976 |
Code of Federal Regulations: Containing a Codification of Documents of ... Uten tilgangsbegrensning - 1982 |
Vanlige uttrykk og setninger
acid action administrative record advisory committee agency amended amounts consistent approval Authority citation revised biological Canthaxanthin cation CDER CDRH chapter clinical color additive D&C Color additive mixtures coloring purposes Compliance conform in identity contain Cosmetic Act D&C Orange D&C Red D&C Yellow Deputy Direc Deputy Director determination diluents Director and Deputy ditive Dockets Management Branch Drug Administration drug application Effective date employee Evaluation Exemption from certification FD&C Federal Acquisition Regulation Federal Food FEDERAL REGISTER filed food additive Food and Drug hearing Identity and specifications issue Lead as Pb lic health listed manufacturing practice matter medical devices ment metics mixtures for coloring mixtures prepared therefrom naphthalenedisulfonic notice paragraph participation party percent person petition presiding officer procedures public disclosure quirements regulations regulatory request restrictions safely sioner sory submitted Subpart tification tion tive tors
Populære avsnitt
Side 267 - food additive" means any substance the intended use of which results or may reasonably be expected to result, directly or indirectly, in its becoming a component or otherwise affecting the characteristics of any food...
Side 441 - Advisory Council on Historic Preservation African Development Foundation Federal Acquisition Regulation Agency for International Development, United States Federal Acquisition Regulation Agricultural Marketing Service Agricultural Research Service Agriculture Department Agricultural Marketing Service Agricultural Research Service Animal and Plant Health Inspection Service Chief Financial Officer, Office of Commodity Credit Corporation Cooperative State Research, Education, and Extension Service Economic...
Side 161 - Although! relevant, evidence may be excluded if its probative value is substantially outweighed by the danger of unfair prejudice, confusion of the Issues, or misleading the Jury, or by considerations of undue delay, waste of time, or needless presentation of cumulative evidence.
Side 179 - ... could reasonably be expected to constitute an unwarranted invasion of personal privacy, d. could reasonably be expected to disclose the identity of a confidential source, including a state, local, or foreign agency or authority or any private institution which furnished information on a confidential basis...
Side 179 - ... would disclose techniques and procedures for law enforcement investigations or prosecutions, or would disclose guidelines for law enforcement investigations or prosecutions if such disclosure could reasonably be expected to risk circumvention of the law...
Side 371 - USP) 2.5. 5, and 10 mg contain FD&C Yellow No. 5 (tartrazine) which may cause allergic-type reactions (including bronchial asthma) in certain susceptible individuals. Although the overall incidence of FD&C Yellow No. 5 (tartrazine) sensitivity in the general population is low, it is frequently seen In patients who also have aspirin hypersensitivity.
Side 164 - Never use any information coming to him confidentially in the performance of governmental duties as a means for making private profit. 9. Expose corruption wherever discovered. 10. Uphold these principles, ever conscious that public office is a public trust.
Side xi - Label" means any display of written, printed, or graphic matter on the immediate container of any article, or any such matter affixed to any consumer commodity or affixed to or appearing upon a package containing any consumer commodity.
Side 272 - Administration has established, and published in the FEDERAL REGISTER, a list of categories of research that may be reviewed by the IRB through an expedited review procedure. The list will be amended, as appropriate, through periodic republication in the FEDERAL REGISTER.
Side 164 - Never discriminate unfairly by the dispensing of special favors or privileges to anyone, whether for remuneration or not; and never accept, for himself or his family, favors or benefits under circumstances which...