The Code of Federal Regulations of the United States of AmericaU.S. Government Printing Office, 1977 The Code of Federal Regulations is the codification of the general and permanent rules published in the Federal Register by the executive departments and agencies of the Federal Government. |
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1.–5. rezultāts no 100.
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NATIONAL ARCHIVES Эн * 1934 * OF THE UNITED STATES 21 Food and Drugs PARTS 200 TO 299 Revised as of April 1 , 1977 code of federal regulations code of federal regulations NATIONAL THE ARCHIVES LCO 1934 OF. Front Cover.
NATIONAL ARCHIVES Эн * 1934 * OF THE UNITED STATES 21 Food and Drugs PARTS 200 TO 299 Revised as of April 1 , 1977 code of federal regulations code of federal regulations NATIONAL THE ARCHIVES LCO 1934 OF. Front Cover.
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... by the Office of the Federal Register National Archives and Records Service General Services Administration as a Special Edition of the Federal Register 1972 for vis federal register code of gulations 7 Agriculture. Basenet TFA.
... by the Office of the Federal Register National Archives and Records Service General Services Administration as a Special Edition of the Federal Register 1972 for vis federal register code of gulations 7 Agriculture. Basenet TFA.
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Explanation The Code of Federal Regulations is a codification of the general and permanent rules published in the Federal Register by the Executive departments and agencies of the Federal Government . The Code is divided into 50 titles ...
Explanation The Code of Federal Regulations is a codification of the general and permanent rules published in the Federal Register by the Executive departments and agencies of the Federal Government . The Code is divided into 50 titles ...
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... Federal Register ( Table II ) . A list of CFR Titles , Chapters , and Parts , an alphabetical list of CFR subtitles and chapters , and lists of current and superseded CFR volumes are also included in this volume . An index to the text ...
... Federal Register ( Table II ) . A list of CFR Titles , Chapters , and Parts , an alphabetical list of CFR subtitles and chapters , and lists of current and superseded CFR volumes are also included in this volume . An index to the text ...
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... regulations codified under this title of the CFR as of April 1 , 1977 . Redesignation tables for Chapter I - Food and Drug Administration appear in the Finding Aids section of the first six volumes . The Code of Federal Regulations is ...
... regulations codified under this title of the CFR as of April 1 , 1977 . Redesignation tables for Chapter I - Food and Drug Administration appear in the Finding Aids section of the first six volumes . The Code of Federal Regulations is ...
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52 Stat acid active ingredient adequate advertisement Agency amended aminopyrine animal drug approved batch beling Bureau chapter chlorcyclizine clinical Code Commission Commissioner of Food contraindications Cosmetic Act cyclizine declaration dispensing distributor dosage form dosage unit Drug Administration drug application drug components Drug Establishment drug listing drug preparations drug product drugs containing equipment established name exempt facture Federal Food Federal Register Food and Drug hexachlorophene information required intended label bears manufac manufacturing practice meclizine medicated feed medicated premix ment milligrams milligrams per dosage name or designation National National Drug Code NDC number new-drug application nitrite inhalant Office oral over-the-counter over-the-counter drug Packaging and labeling packer paragraph pernicious anemia potassium potassium permanganate prescription drug principal display panel processing proprietary name quantity of contents records regarded as misbranded regulatory revised safety Secs Service shipment side effects specific statement subject to section submitted SUBTITLE taining tion Title warning
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23. lappuse - Labeling on or within the package from which the drug is to be dispensed bears adequate information for its use, including indications, effects, dosages, routes, methods, and frequency and duration of administration, and any relevant hazards, contraindications, side effects, and precautions...
97. lappuse - drug defined in an official compendium" means a drug having the identity prescribed for a drug in an official compendium. (c) A statement that a drug defined in an official compendium differs in strength, quality, or purity from the standard of strength, quality, or purity set forth for such drug in an official compendium shall show all the respects in which such drug so differs, and the extent of each such difference.
23. lappuse - ... because of its toxicity or other potentiality for harmful effect, or the method of its use, or the collateral measures necessary to its use, is not safe for use except under the supervision of a practitioner licensed by law to administer such drug...
27. lappuse - Act (1) small open containers of fresh fruits and fresh vegetables and (2) food which is, in accordance with the practice of the trade, to be processed, labeled, or repacked in substantial quantities at establishments other than those where originally processed or packed, on condition that such food is not adulterated or misbranded under the provisions of this Act upon removal from such processing, labeling, or repacking establishment.
35. lappuse - The same information concerning the ingredients of the drug as appears on the label and labeling on or within the package from which the drug is to be dispensed...
31. lappuse - INDICATIONS Based on a review of this drug by the National Academy of SciencesNational Research Council and/or other information, FDA has classified the indications as follows: Effective: For the management of the manifestations of psychotic disorders.
28. lappuse - ... during the time of introduction into and movement in interstate commerce and the time of holding in such establishment, from compliance with the labeling requirements of...
13. lappuse - English. (2) If the label contains any representation in a foreign language, all words, statements, and other information required by or under authority of the act to appear on the label shall appear thereon in the foreign language. (3) If the...
26. lappuse - If a shipment or delivery, or any part thereof, of a drug or device which is exempt under the regulations in this section is made to a person in whose possession the article is not exempt, or is made for any purpose other than those specified, such exemption shall expire, with respect to such shipment or delivery or part thereof, at the beginning of that shipment or delivery.
25. lappuse - In vitro diagnostic products. (a) "In vitro diagnostic products" are those reagents, instruments and systems intended for use in the diagnosis of disease or in the determination of the state of health in order to cure, mitigate, treat, or prevent disease or its sequelae. Such products are intended for use in the collection, preparation and examination of specimens taken from the human body. These products are drugs or devices as defined in section...