§500.25. Anthelmintic drugs for use in animals. — Inbound Citations
21 C.F.R. § 500.25
Statutory Authority
Cited by 30 regulations in release Current.
Citations to 21 U.S.C. § 500.25 as a whole
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(d) See § 500.25 of this chapter.
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(c) See § 500.25 of this chapter.
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(d) See § 500.25 of this chapter.
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(c) See § 500.25 of this chapter.
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(d) See § 500.25 of this chapter.
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(c) See § 500.25 of this chapter.
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(c) See § 500.25 of this chapter.
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(d) See § 500.25 of this chapter.
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(d) See § 500.25 of this chapter. If labeled for administration by stomach tube: Federal law restricts this drug to use by or on the order of a licensed veterinarian.
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(1) See § 500.25 of this chapter.
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(c) See § 500.25 of this chapter.
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(c) See § 500.25 of this chapter.
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(c) See § 500.25 of this chapter.
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(d) See § 500.25 of this chapter.
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(1) See § 500.25 of this chapter.
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(c) See § 500.25 of this chapter.
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(d) See § 500.25 of this chapter.
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(1) See § 500.25 of this chapter.
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(d) See § 500.25 of this chapter.
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(d) See § 500.25 of this chapter.
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(1) One mL per 22 pounds (0.5 milligram per kilogram) of body weight applied topically to the back of the animal.(2) It is used for the treatment and control of: Gastrointestinal roundworms (adults and fourth-stage larvae) Ostertagia ostertagi (including inhibited stage), Haemonchus placei, Trichostrongylus axei, T. colubriformis, Cooperia oncophora, C. punctata, C. surnabada, Oesophagostomum radiatum (adults); Strongyloides papillosus, Trichuris spp.; lungworms (adults and fourth-stage larvae) Dictyocaulus viviparus; cattle grubs (parasitic stages) Hypoderma bovis, H. lineatum; mites Sarcoptes scabiei var. bovis; lice Linognathus vituli, Haematopinus eurysternus, Damalinia bovis, Solenoptes capillatus; and horn flies Haematobia irritans. It controls infections and prevents reinfection with O. radiatum and D. viviparus for 28 days after treatment, C. punctata and T. axei for 21 days after treatment, O. ostertagi, H. placei, C. oncophora, and C. surnabada for 14 days after treatment, and D. bovis for 56 days after treatment.(3) Do not treat cattle within 48 days of slaughter. Do not use on female dairy cattle of breeding age or on calves to be processed for veal. Consult your veterinarian for assistance in the diagnosis, treatment, and control of parasitism.
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(iii) A withdrawal period has not been established for this product on preruminating calves. Do not use on calves to be processed for veal. See § 500.25 of this chapter.
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(d) See § 500.25 of this chapter.
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(d) See § 500.25 of this chapter.
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(1) Labeling shall bear the following warning: The active ingredient coumaphos is a cholinesterase inhibitor. Do not use this product on animals simultaneously or within a few days before or after treatment with, or exposure to, cholinesterase-inhibiting drugs, pesticides, or chemicals.(2) See § 500.25 of this chapter.
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(d) See § 500.25 of this chapter.
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(d) See § 500.25 of this chapter.
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(1) See § 500.25 of this chapter. Consult a veterinarian before using in severely debilitated animals.
Citations to §500.25(c)
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(c) See § 500.25(c) of this chapter.