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Code of Federal Regulations (Last Updated: November 8, 2024) |
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Title 21 - Food and Drugs |
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Chapter I - Food and Drug Administration, Department of Health and Human Services |
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SubChapter E - Animal Drugs, Feeds, and Related Products |
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Part 556 - Tolerances for Residues of New Animal Drugs in Food |
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Subpart B - Specific Tolerances for Residues of Approved and Conditionally Approved New Animal Drugs |
§ 556.425 - Morantel.
Latest version.
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§ 556.425 Morantel tartrate.
A tolerance of 0.7 part per million is established.
(a) Acceptable daily intake (ADI). The ADI for total residue of morantel tartrate is 10 µg/kg of body weight per day.
MAPA,(b) Tolerances. The tolerances for N-methyl-1,3-propanediamine (
in the liver (marker residue)
of cattle and goats. A tolerance for residues of morantel tartrate in milk is not required.are:
(1) Cattle.
(i) Liver (target tissue)
[59 FR 17922, Apr. 15, 1994]
: 0.7 ppm.
(ii) Milk: Not required.
(2) Goats.
(i) Liver (target tissue): 0.7 ppm.
(ii) Milk: Not required.
(c) Related conditions of use. See §§ 520.1450a, 520.1450b, 520.1450c, and 558.360 of this chapter.