The Code of Federal Regulations of the United States of AmericaU.S. Government Printing Office, 1993 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 56.
4. lappuse
... dosage information . 200.10 Contract facilities ( including con- sulting laboratories ) utilized as extramu- ral facilities by pharmaceutical manu- facturers . 200.11 Use of octadecylamine in steam lines of drug establishments . 200.15 ...
... dosage information . 200.10 Contract facilities ( including con- sulting laboratories ) utilized as extramu- ral facilities by pharmaceutical manu- facturers . 200.11 Use of octadecylamine in steam lines of drug establishments . 200.15 ...
5. lappuse
... dosage information . There are presently no regulations under the Federal Food , Drug , and Cosmetic Act that prevent a manufac- turer of prescription drugs from send- ing the pharmacist data he needs on indications and dosage in ...
... dosage information . There are presently no regulations under the Federal Food , Drug , and Cosmetic Act that prevent a manufac- turer of prescription drugs from send- ing the pharmacist data he needs on indications and dosage in ...
6. lappuse
... dosage form that con- tains per dosage unit ( for example , capsule or tablet ) , a quantity of active drug ingredients which is not general- ly recognized as safe for administra- tion as a single dose under the condi- tions suggested ...
... dosage form that con- tains per dosage unit ( for example , capsule or tablet ) , a quantity of active drug ingredients which is not general- ly recognized as safe for administra- tion as a single dose under the condi- tions suggested ...
8. lappuse
... dosage form ; and the price charged for a prescription for a specific quantity of the drug product . ( 3 ) The reminder advertisement or reminder labeling may also include other written , printed , or graphic matter , e.g. ...
... dosage form ; and the price charged for a prescription for a specific quantity of the drug product . ( 3 ) The reminder advertisement or reminder labeling may also include other written , printed , or graphic matter , e.g. ...
9. lappuse
... dosage . 201.56 General requirements on content and format of labeling for human pre- scription drugs . 201.57 Specific requirements on content and format of labeling for human pre- scription drugs . 201.58 Requests for waiver of ...
... dosage . 201.56 General requirements on content and format of labeling for human pre- scription drugs . 201.57 Specific requirements on content and format of labeling for human pre- scription drugs . 201.58 Requests for waiver of ...
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active ingredient adequate advertisement amended appropriate approved batch bear beling cation chapter chlorcyclizine clinical closures cluding Code contraindications control number Cosmetic Act cyclizine detoxification distribution distributor dosage form dose Drug Administration drug application Drug Enforcement Administration drug establishment drug listing drug prod drug product containers equipment established name evaluation exemption expiration date facture Federal Food Federal Register Food and Drug gram hexachlorophene intended licensed maintenance treatment manu manufac manufacturing meclizine medicated article(s medicated feed ment Methadone misbranded name or designation narcotic narcotic drugs National Office operations oral over-the-counter over-the-counter drug packaging and labeling packing paragraph patient patient's record pernicious anemia person potassium permanganate pregnancy Pregnancy category preparations prescription drugs principal display panel processing program physician proprietary name quired regulations safety sample shipment side effects specific storage submitted Subpart tained testing tients tion treatment program ture Type A medicated ucts
Populāri fragmenti
45. lappuse - Indications Based on a review of this drug by the National Academy of Sciences — National Research Council and/or other information, FDA has classified the indications as follows: Effective: For the management of the manifestations of psychotic disorders.
23. 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 - ProHance* should be used during pregnancy only if the potential benefit justifies the potential risk to the fetus.
25. 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.
38. 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...
x. lappuse - All prices include regular domestic postage and handling and are subject to change. (Company or personal name) (Additional address/attention line) (Street address) 3.
53. 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...
42. lappuse - REGULATIONS MAKING EXEMPTIONS SEC. 405. The Secretary shall promulgate regulations exempting from any labeling requirement of this 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...
25. 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...
16. 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.