Code of Federal Regulations: Containing a Codification of Documents of General Applicability and Future Effect as of December 31, 1948, with Ancillaries and IndexU.S. General Services Administration, National Archives and Records Service, Office of the Federal Register, 2001 Special edition of the Federal Register, containing a codification of documents of general applicability and future effect ... with ancillaries. |
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active ingredient adequate advertisement amended appropriate approved Authority citation revised batch beling chapter clinical Code components control number Cosmetic Act Department dispensed distribution dosage form dose Drug Administration drug application Drug Facts drug listing drug prod drug products containing drug sample equipment established name exemption facture Federal Acquisition Regulation Federal Food Federal Register Food and Drug health care entity hexachlorophene human intended labeling maintenance treatment manufac manufacturer manufacturing practice medicated article(s medicated feed Medication Guide ment methadone misbranded name or designation narcotic narcotic drugs National National Drug Code Office oral OTC drug products over-the-counter over-the-counter drug package Packaging and labeling paragraph patient pediatric person Pregnancy Category prescription drug procedures program physician proprietary name quantity quired request safety Service sodium specific storage Subpart taining tamper-evident tartrazine testing tion Title Type A medicated unit warning statement
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22. lappuse - ProHance* should be used during pregnancy only if the potential benefit justifies the potential risk to the fetus. 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 ProHance' is administered to a nursing woman.
201. lappuse - 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...
23. 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.
15. 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.
22. 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...
24. 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...
49. 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...
184. lappuse - LIX National Aeronautics and Space Administration (Part 6901) LX United States Postal Service (Part 7001) LXI National Labor Relations Board (Part 7101...
52. 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.
183. lappuse - Title 1— General Provisions I Administrative Committee of the Federal Register (Parts 1 — 49) II Office of the Federal Register (Parts 50—299) IV Miscellaneous Agencies (Parts 400 — 500) Title 2— Grants and Agreements SUBTITLE A— OFFICE OF MANAGEMENT AND BUDGET GUIDANCE FOR GRANTS AND AGREEMENTS I...