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21 CFR 522.1079

§ 522.1079 Serum gonadotropin and chorionic gonadotropin.

United States · 21 CFR — Food and Drugs · Status: effective

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21 CFR 522.1079, § 522.1079 Serum gonadotropin and chorionic gonadotropin, United States, version 1 as recorded 2026-07-09, yourstate.us, https://yourstate.us/provision/87456
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(a) Specifications. Each dose consists of 400 international units (I.U.) serum gonadotropin and 200 I.U. chorionic gonadotropin as a freeze-dried powder to be reconstituted with 5 milliliters of sterile aqueous diluent. (b) Sponsor. See No. 000061 in § 510.600(c) of this chapter. (c) Related tolerances. See § 556.304 of this chapter. (d) Conditions of use in swine—(1) Amount. 400 I.U. serum gonadotropin with 200 I.U. chorionic gonadotropin per 5 milliliters dose per animal. (2) Indications for use—(i) Gilts. For induction of fertile estrus (heat) in healthy prepuberal (noncycling) gilts. (ii) Sows. For induction of estrus in healthy weaned sows experiencing delayed return to estrus. (3) Limitations. For subcutaneous use only. (i) Gilts. For use only in gilts over 5 1/2 months of age and weighing at least 85 kilograms (187 pounds). (ii) Sows. Delayed return to estrus is most prevalent after the first litter. The effectiveness has not been established after later litters. Delayed return to estrus often occurs during periods of adverse environmental conditions, and sows mated under such conditions may farrow smaller than normal litters.

Legislative history

This is a federal regulation, adopted through agency rulemaking under the Administrative Procedure Act — not enacted by a recorded vote of Congress.