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" Formulary, it differs from the standard of strength, quality, or purity, as determined by the test laid down in the United States Pharmacopoeia or National Formulary official at the time of investigation: Provided, That no drug defined in the United States... "
The Food and Drugs Act, June 30, 1906: A Study with Text of the Act ... - Сторінка 76
автори: Arthur Philip Greeley - 1907 - 176 стор.
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Acts Passed at the ... Session of the General Assembly for the Commonwealth ...

Kentucky - 1918 - 808 стор.
...down in the United States Pharmacopoeia' or National Formulary official at the time of investigation. Provided, that no drug defined in the United States...thereof, although the standard may differ from that made by the test laid down in the United States Pharmacopoeia or National Formulary. Second. If the...
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Biennial report of the Louisiana State Board of Health. 1906/07

1908 - 696 стор.
...down in the United States Pharmacopoeia or National Formulary official at the time of investigation: Provided, That no drug defined in the United States...from that determined by the test laid down in the Unites States Pharmacopoeia or National Formulary. Second. If its strength or purity fall below the...
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The Tribune Almanac and Political Register

1907 - 396 стор.
...defined in the United Stales Pharmacopoeia or National Formulary shall be deemed to be adulterated thix provision if the standard of strength, quality or purity be plainly stated Ihfe bottle, box "or other container thereof, although the ertandard may differ from bat determined...
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The Medical Brief: A Monthly Journal of Scientific Medicine and Surgery, Том 38

1910 - 806 стор.
...down by the United States Pharmacopoeia or National Formulary official at the time of investigation ; Provided, That no drug defined in the United States...down in the United States Pharmacopoeia or National Formulary. If the Coudrey amendment is enacted according to his proposal, it will make this clause...
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Public health reports (1881). v. 28 pt. 2 no. 27-52, 1913

1914 - 1550 стор.
...down by the United States Pharmacopoeia or National Formulary official at the time of investigation: Provided, That no drug defined in the United States...down in the United States Pharmacopoeia or National Formulary." Sec. 739 (as amended). "That a flavoring extract is a solution iu ethyl alcohol of proper...
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Meyer Brothers Druggist, Том 36

1915 - 464 стор.
...therein. 2. If its strength, quality or purity fall below the professed standard under which it is sold: Provided, that no drug defined in the United States...plainly stated upon the bottle, box or other container thereof,"although the standard may differ from that determined by the test laid down in the United...
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The Medical Fortnightly, Томи 29 – 30

1906 - 760 стор.
...official at the time of investigation; Provided, That no drug defined in the United States Pharmacopeia or National Formulary shall be deemed to be adulterated...container thereof, although the standard may differ irom that determined by the test laid down in the United States Pharmacopeia . or National Formulary....
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Hygienic Laboratory bulletin. no. 106-109, 1916-17, Випуски 106 – 109

1917 - 684 стор.
...down in the United States Pharmacopoeia or National Formulary official at the time of investigation: Provided, That no drug defined in the United States...standard may differ from that determined by the test hud down in the United States Pharmacopoeia or in the National Formulary. During the decade that has...
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Hygienic Laboratory bulletin. no. 41, 1908, Випуск 41

1908 - 842 стор.
...official at the time of investigation : Provided. That no drug defined in the United States Pharmacopeia or National Formulary shall be deemed to be adulterated...of strength, quality, or purity be plainly stated u|K>n the bottle, hox, or other container thereof although the standard may differ from that determined...
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Transactions of the Kansas Academy of Science, Томи 20 – 21

Kansas Academy of Science - 1906 - 918 стор.
...Pharmacopoeia or National Formulary, they differ from the standard of strength, purity or quality as determined by the test laid down in the United States Pharmacopoeia or National Formulary official at the time of investigation." Provision is made whereby these drugs may not be...
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