Complete Up To Date Information about Banamine®-S.
NADA Number: 101-479 | |
| Proprietary Name |
Banamine®-S Banamine® Injectable Solution |
|---|---|
| Sponsor |
Schering-Plough Animal Health Corp. |
| Sponsor Address |
P.O. Box 21 Sandown Village, NJ 3171 VIC Australia |
| Ingredients |
Flunixin Meglumine |
| Species |
Horse, not for meat production Cattle, beef Cattle, dairy, lactating Cattle, dairy, heifers not lactating Cattle, calves, excluding veal calves Swine, no use class stated or implied |
| Routes of Administration |
Intravenous Intramuscular (swine) Intramuscular (horse) |
| Dose Form |
Liquid (solution) |
| Drug Form |
Liquid (solution) |
| Dispensing Status |
RX |
| Patent Number |
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| Exclusivity |
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| Withdrawal Time |
Cattle: 4 days before slaughter. A withdrawal time for pre-ruminating veal calves has not been established.
Milk: 36 hours
Swine: 12 days before slaughter. |
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Dosage Amount, Indications & Limitations |
Flunixin meglumine solution. Specifications: The drug contains 50 milligrams of flunixin per milliliter of aqueous solution. Conditions of use: Horses Amount: 0.5 mg per pound of body weight per day, intravenously or intramuscularly, for up to 5 days. Indications: For alleviation of inflammation and pain associated with musculoskeletal disorders, and alleviation of pain associated with colic. Limitations: Not for use in horses intended for food. Federal law restricts this drug to use by or on the order of a licensed veterinarian. Cattle Amount: 1.1 to 2.2 mg/kilogram (0.5 to 1.0 mg/lb) of body weight per day, as a single dose or divided into 2 doses administered at 12-hour intervals, intravenously, for up to 3 days. Alternatively, 2.2 mg/kg (1.0 mg/lb) of body weight given once by intravenous administration. Indications: For control of pyrexia associated with bovine respiratory disease, acute bovine mastitis, and endotoxemia. Also indicated for control of inflammation in endotoxemia. Limitations. Do not slaughter for food use within 4 days of last treatment. A withdrawal period has not been established for use in preruminating calves. Do not use in calves to be processed for veal. Do not use in dry dairy cows. Milk that has been taken during treatment and for 36 hours after the last treatment must not be used for food. Federal law restricts this drug to use by or on the order of a licensed veterinarian. Swine For product labeled under Banamine®-S: Amount: Administer 2.2 mg/kilogram (1.0 mg/lb) of body weight as a single intramuscular injection. Indications: For the control of pyrexia associated with swine respiratory disease. Limitations: Swine must not be slaughtered for human consumption within 12 days of last treatment. Federal law restricts this drug to use by or on the order of a licensed veterinarian.
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| Tolerances |
Cattle The tolerance flunixin free acid is: a. Liver (target tissue) 125 parts per billion (ppb). b. Muscle 25 ppb. c. Milk 2 ppb. Swine The tolerance flunixin free acid is: a. Liver (target tissue) 30 ppb. b. Muscle 25 ppb.
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