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 |
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1.–5. rezultāts no 60.
. lappuse
... Title 21 pt . 200-299 2000 University of Michigan Documents Center Code of Federal Regulation Food and Drugs UNIVERSITY OF MICHIGAN LIBRARIES AUG 0 3 2000 DEPOSITED BY UNITED STATES OF AMERICA Sec . PART 200 - GENERAL Subpart A ...
... Title 21 pt . 200-299 2000 University of Michigan Documents Center Code of Federal Regulation Food and Drugs UNIVERSITY OF MICHIGAN LIBRARIES AUG 0 3 2000 DEPOSITED BY UNITED STATES OF AMERICA Sec . PART 200 - GENERAL Subpart A ...
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... Ancillaries and Index. U.S. GOVERNMENT PRINTING OFFICE WASHINGTON : 2000 For sale by U.S. Government Printing Office Superintendent of Documents , Mail Stop : SSOP , Washington , DC 20402-9328 Explanation Title 21 : Chapter I - Food and ...
... Ancillaries and Index. U.S. GOVERNMENT PRINTING OFFICE WASHINGTON : 2000 For sale by U.S. Government Printing Office Superintendent of Documents , Mail Stop : SSOP , Washington , DC 20402-9328 Explanation Title 21 : Chapter I - Food and ...
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... Title 21 : Chapter I - Food and Drug Administration , Department of Health and Human Services ( Continued ) Finding Aids : Page V 3 Material Approved for Incorporation by Reference 183 Table of CFR Titles and Chapters 185 Alphabetical ...
... Title 21 : Chapter I - Food and Drug Administration , Department of Health and Human Services ( Continued ) Finding Aids : Page V 3 Material Approved for Incorporation by Reference 183 Table of CFR Titles and Chapters 185 Alphabetical ...
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... title , part and section num- ber . Thus , 21 CFR 200.5 refers to title 21 , part 200 , section 5 . The Code of Federal Regulations is a codification of the iv Title.
... title , part and section num- ber . Thus , 21 CFR 200.5 refers to title 21 , part 200 , section 5 . The Code of Federal Regulations is a codification of the iv Title.
v. lappuse
... title is divided into chapters which usually bear the name of the issuing agency . Each chapter is further sub ... Title 1 through Title 16 ...... Title 17 through Title 27 Title 28 through Title 41 Title 42 through Title 50 .. .as of ...
... title is divided into chapters which usually bear the name of the issuing agency . Each chapter is further sub ... Title 1 through Title 16 ...... Title 17 through Title 27 Title 28 through Title 41 Title 42 through Title 50 .. .as of ...
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active ingredient adequate administered or dispensed advertisement amended appropriate approved Authority citation revised batch beling chapter clinical Code components Cosmetic Act Department detoxification distribution dosage form dose Drug Administration drug application Drug Establishment Drug Facts drug listing drug prod drug products containing drug sample effective equipment established name evaluation exemption Federal Acquisition Regulation Federal Food Federal Register Food and Drug hexachlorophene human labeling licensed practitioner manufac manufacturer manufacturing practice medicated article(s medicated feed Medication Guide ment methadone milligrams misbranded narcotic drugs National National Drug Code Office oral OTC drug products over-the-counter drug package Packaging and labeling paragraph patient patient's record pediatric person Pregnancy Category pregnant prescription drug procedures program physician proprietary name quantity quired request responsible Service sodium specific submitted taining take-home medication tamper-evident tients tion treatment plan treatment program Type A medicated unit
Populāri fragmenti
18. lappuse - There are. however, no adequate and well-controlled studies in pregnant women. Because animal reproduction studies are not always predictive of human response, this drug should be used during pregnancy only if clearly needed...
10. lappuse - 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.
18. lappuse - ProHance* should be used during pregnancy only if the potential benefit justifies the potential risk to the fetus.
19. lappuse - Because many drugs are excreted in human milk and because of the potential for serious adverse reactions in nursing infants from Lortab 7.5/500 tablets, a decision should be made whether to discontinue nursing or to discontinue the drug, taking into account the importance of the drug to the mother.
45. 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...
19. lappuse - Nursing Mothers: It is not known whether this drug is excreted in human milk. Because many drugs are excreted in human milk, caution should be exercised when sucralfate is administered to a nursing woman.
58. 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...
173. lappuse - Office of the Assistant Secretary for Housing — Federal Housing Commissioner, Department of Housing and Urban Development (Section 8 Housing Assistance Programs, Section 202 Direct Loan Program, Section 202 Supportive Housing for the Elderly Program and Section 811 Supportive Housing for Persons With Disabilities Program) (Parts 800—899) IX Office of Assistant Secretary for Public and Indian Housing, Department of Housing and Urban Development (Parts 900—999...
48. 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.
173. lappuse - Bureau of Land Management, Department of the Interior (Parts 1000—9999) III Utah Reclamation Mitigation and Conservation Commission (Parts...