21 CFR 520.88f

§ 520.88f Amoxicillin trihydrate tablets.

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

Cite this

Citation: 21 CFR 520.88f, § 520.88f Amoxicillin trihydrate tablets, United States, version 1 as recorded 2026-07-09, yourstate.us, https://yourstate.us/provision/87075
Permanent ID: ys:prov:87075@1
SHA-256: 05c00ed2d430b4ad6795568d95487045d98ff25dbd04758e76c004aa4bb6ca94

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Full text

(a) Specifications. Each tablet contains amoxicillin trihydrate equivalent to 50, 100, 200, or 400 milligrams (mg) amoxicillin. (b) Sponsors. See Nos. 051311 and 054771 in § 510.600(c) of this chapter. (c) Conditions of use in dogs—(1) Amount. Administer 5 mg per pound of body weight twice daily for 5 to 7 days or 48 hours after all symptoms have subsided. (2) Indications for use. For treatment of bacterial dermatitis due to Staphylococcus aureus, Streptococcus spp., Staphylococcus spp., and Escherichia coli; and soft tissue infections (abscesses, wounds, lacerations) due to S. aureus, Enterococcus faecalis, E. coli, Proteus mirabilis, and Staphylococcus spp. (3) Limitations. Federal law restricts this drug to use by or on the order of a licensed veterinarian.

Legislative history

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