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, 1997 Special edition of the Federal Register, containing a codification of documents of general applicability and future effect ... with ancillaries. |
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1.5. rezultāts no 42.
6. lappuse
... application pur- suant to section 505 of the act is there- fore a prerequisite to interstate ship- ment of such articles , except as pro- vided by section 505 ( i ) . §200.31 Timed release dosage forms . ( a ) Many drugs are now being ...
... application pur- suant to section 505 of the act is there- fore a prerequisite to interstate ship- ment of such articles , except as pro- vided by section 505 ( i ) . §200.31 Timed release dosage forms . ( a ) Many drugs are now being ...
11. lappuse
... application . ( d ) Duration of administration or ap- plication . ( e ) Time of administration or appli- cation ( in relation to time of meals , time of onset of symptoms , or other time factors ) . ( f ) Route or method of administra ...
... application . ( d ) Duration of administration or ap- plication . ( e ) Time of administration or appli- cation ( in relation to time of meals , time of onset of symptoms , or other time factors ) . ( f ) Route or method of administra ...
29. lappuse
... application or abbreviated new drug application under section 505 of the act or ( iii ) an anti- biotic drug subject to an approved anti- biotic form , §§ 201.56 , 201.57 , and 201.100 ( d ) ( 3 ) are effective on the date listed below ...
... application or abbreviated new drug application under section 505 of the act or ( iii ) an anti- biotic drug subject to an approved anti- biotic form , §§ 201.56 , 201.57 , and 201.100 ( d ) ( 3 ) are effective on the date listed below ...
37. lappuse
... application or required as a condi- tion for the certification or the exemp- tion from certification requirements applicable to preparations of insulin or antibiotic drugs . ( d ) Any labeling , as defined in section 201 ( m ) of the ...
... application or required as a condi- tion for the certification or the exemp- tion from certification requirements applicable to preparations of insulin or antibiotic drugs . ( d ) Any labeling , as defined in section 201 ( m ) of the ...
40. lappuse
... application under section 505 of the act is approved with respect to such drug but it complies with section 505 ( 1 ) or 512 of the act and regulations thereunder . No exemption shall apply to any other drug which would be a new drug if ...
... application under section 505 of the act is approved with respect to such drug but it complies with section 505 ( 1 ) or 512 of the act and regulations thereunder . No exemption shall apply to any other drug which would be a new drug if ...
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active ingredient adequate advertisement Agency amended animal appropriate approved Authority citation batch beling chapter clinical closures Code Commission components contraindications control number Cosmetic Act Department detoxification distribution distributor dosage form dose Drug Administration drug application drug listing drug product containers equipment established name evaluation exemption Federal Acquisition Regulation Federal Food Federal Register Food and Drug gram Health hexachlorophene human intended licensed maintenance treatment manufac manufacture manufacturing practice medicated article(s medicated feed ment methadone misbranded name or designation narcotic narcotic drugs National National Drug Code new-drug Office operations oral over-the-counter drug package Packaging and labeling paragraph patient patient's record pediatric pernicious anemia person pregnancy Pregnancy Category prescription drugs processing program physician proprietary name quired safety sample Service shipment specific storage submitted Subpart SUBTITLE tained tainer testing tion treatment program Type A medicated ucts unit warning statement
Populāri fragmenti
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...
23. lappuse - ProHance* should be used during pregnancy only if the potential benefit justifies the potential risk to the fetus.
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.
24. 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.
39. 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...
156. lappuse - Overseas Private Investment Corporation (Part 4301) XXXV Office of Personnel Management (Part 4501) XL Interstate Commerce Commission (Part 5001) XLI Commodity Futures Trading Commission (Part 5101...
43. 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...
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...
24. lappuse - If a patient becomes pregnant while taking this drug, the patient should be apprised of the potential hazard to the fetus.
38. lappuse - ... that furnishes or purports to furnish information for use or which prescribes, recommends, or suggests a dosage for the 21 CFR Ch.