Complete Up To Date Information about Tripelennamine Hydrochloride Injection.
ANADA Number: 200-162 | |
| Proprietary Name |
Tripelennamine Hydrochloride Injection |
|---|---|
| Sponsor |
Teva Animal Health, Inc. |
| Sponsor Address |
3915 South 48th Street Ter. St. Joseph, MO 64506 USA |
| Ingredients |
Tripelennamine Hydrochloride |
| Species |
Cattle, excluding veal calves Horse, not for meat production |
| Routes of Administration |
Intravenous (cattle) Intramuscular |
| Dose Form |
Liquid (solution) |
| Drug Form |
Liquid (solution) |
| Dispensing Status |
RX |
| Withdrawal Time |
Cattle: 4 days before slaughter. A withdrawal time for pre-ruminating veal calves has not been established.
Milk: 24 hours. |
|
Dosage Amount, Indications & Limitations |
522.2615 Tripelennamine hydrochloride injection. Specifications: Each milliliter of aqueous solution contains 20 milligrams of tripelennamine hydrochloride. Conditions of use: Horses Amount: Administer intramuscularly at a dose of 0.5 milligram per pound of body weight. Indications: For use in treating conditions in which antihistaminic therapy may be expected to lead to alleviation of some signs of disease. Limitations: Do not use in horses intended for food purposes. Federal law restricts this drug to use by or on the order of a licensed veterinarian. Cattle Amount: Administer intravenously or intramuscularly at a dose of 0.5 milligram per pound of body weight. Indications: For use in treating conditions in which antihistaminic therapy may be expected to lead to alleviation of some signs of disease. Limitations: Treated cattle must not be slaughtered for food during treatment and for 4 days following the last treatment. Milk that has been taken during treatment and for 24 hours (2 milkings) after the last treatment must not be used for food. A withdrawal time has not been established for this product in preruminating calves. Do not use in calves to be processed for veal. Federal law restricts this drug to use by or on the order of a licensed veterinarian. NAS/NRC status: These conditions are NAS/NRC reviewed and deemed effective. Applications for these uses need not include effectiveness data as specified by 514.111 of the Code of Federal Regulations Chapter 21, but may require bioequivalency and safety data. |
| Tolerances |
A tolerance of 200 parts per billion (ppb) is established for residues of tripelennamine in uncooked edible tissues of cattle and 20 ppb in milk. |