Complete Up To Date Information about Nuflor Gold™.
NADA Number: 141-265 | |
| Proprietary Name |
Nuflor Gold™ |
|---|---|
| Sponsor |
Schering-Plough Animal Health Corp. |
| Sponsor Address |
P.O. Box 21 Sandown Village, NJ 3171 VIC Australia |
| Ingredients |
Florfenicol |
| Species |
Cattle, beef Cattle, dairy, females under 20 months of age |
| Routes of Administration |
Subcutaneous |
| Dose Form |
Liquid (solution) |
| Drug Form |
Liquid (solution) |
| Dispensing Status |
RX |
| Exclusivity |
Newly formulated product containing additional inactive ingredients. |
| Withdrawal Time |
44 days. |
|
Dosage Amount, Indications & Limitations |
522.955 Florfenicol. Specifications. Each milliliter (mL) of solution contains 300 milligrams (mg) florfenicol in the inactive vehicles 2-pyrrolidone and triacetin. Conditions of use. Cattle (beef and non-lactating dairy cattle) Amount: 40 mg/kilogram (kg) body weight as a single subcutaneous injection. Indications: For treatment of bovine respiratory disease (BRD) associated with Mannheimia haemolytica, Pasteurella multocida, and Histophilus somni in beef and non-lactating dairy cattle. Limitations: Do not slaughter within 44 days of last treatment. Do not use in female dairy cattle 20 months of age or older. Use may cause milk residues. A withdrawal period has not been established 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. |
| Tolerances |
Cattle a. Liver (the target tissue). The tolerance for florfenicol amine (the marker residue) is 3.7 parts per million (ppm). b. Muscle. The tolerance for florfenicol amine (the marker residue) is 0.3 ppm. Swine a. Liver (the target tissue). The tolerance for parent florfenicol (the marker residue) is 2.5 ppm. b. Muscle. The tolerance for parent florfenicol (the marker residue) is 0.2 ppm. |