GroundRules
21 CFR 556.735: Tilmicosin.
Where this section sits in the code
- Title 21—Food and Drugs
- CHAPTER I—FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES
- SUBCHAPTER E—ANIMAL DRUGS, FEEDS, AND RELATED PRODUCTS
- PART 556—TOLERANCES FOR RESIDUES OF NEW ANIMAL DRUGS IN FOOD
- Subpart B—Specific Tolerances for Residues of Approved and Conditionally Approved New Animal Drugs
(a) Acceptable daily intake (ADI). The ADI for total residue of tilmicosin is 25 µg/kg of body weight per day.
(b) Tolerances. The tolerances for tilmicosin (marker residue) are:
(1) Cattle. (i) Liver (target tissue): 1.2 ppm.
(ii) Muscle: 0.1 ppm.
(2) Sheep. (i) Liver (target tissue): 1.2 ppm.
(ii) Muscle: 0.1 ppm.
(3) Swine. (i) Liver (target tissue): 7.5 ppm.
(ii) Muscle: 0.1 ppm.
(c) Related conditions of use. See §§ 520.2471, 522.2471, and 558.618 of this chapter.
Collected 2026-08-27T02:24:47Z. Source file · JSON