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21 CFR 520.2605

§ 520.2605 Trimeprazine and prednisolone capsules.

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

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21 CFR 520.2605, § 520.2605 Trimeprazine and prednisolone capsules, United States, version 1 as recorded 2026-07-09, yourstate.us, https://yourstate.us/provision/87368
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(a) Specifications. Each capsule contains: (1) 3.75 milligrams (mg) trimeprazine in sustained released form (as trimeprazine tartrate) and 1 mg prednisolone (Capsule No. 1); or (2) 7.5 mg trimeprazine in sustained release form (as trimeprazine tartrate) and 2 mg prednisolone (Capsule No. 2). (b) Sponsor. See No. 054771 in § 510.600(c) of this chapter. (c) Conditions of use in dogs—(1) Amount. Administer orally once daily an initial dosage: (i) For dogs weighing up to 10 pounds: one Capsule No. 1; (ii) For dogs weighing 11 to 20 pounds, one Capsule No. 2 or two Capsule No. 1; (iii) For dogs weighing 21 to 40 pounds, two Capsule No. 2 or four Capsule No. 1; and (iv) For dogs weighing over 40 pounds, three Capsule No. 2 or six Capsule No. 1. After 4 days, the dosage is reduced to approximately 1/2 the initial dosage or to an amount just sufficient to maintain remission of symptoms. (2) Indications for use. For the relief of itching regardless of cause; and for reduction of inflammation commonly associated with most skin disorders of dogs such as eczema, caused by internal disorders, otitis, and dermatitis, allergic, parasitic, pustular and nonspecific. As adjunctive therapy in various cough conditions including treatment of “kennel cough” or tracheobronchitis, bronchitis including allergic bronchitis, in tonsillitis, acute upper respiratory infections and coughs of nonspecific origin. (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.