ANADA Number: 200-388 |
|
| Proprietary Name |
GB Topical Spray |
|---|---|
| Sponsor |
American Pharmaceuticals and Cosmetics, Inc. |
| Sponsor Address |
1401 Joel East Road Fort Worth, Texas 76140 |
| Ingredients |
GENTAMICIN SULFATE BETAMETHASONE VALERATE |
| Drug Form |
SOLUTION |
| Dispensing Status |
RX |
| Specifications |
Amount: Each mL contains: gentamicin sulfate, USP equivalent to 0.57 mg gentamicin base and betamethasone valerate, USP equivalent to 0.284 mg betamethasone. |
|
Dosage Amount, Indications & Limitations |
Each mL contains: gentamicin sulfate, USP equivalent to 0.57 mg gentamicin base, and betamethasone valerate, USP equivalent to 0.284 mg betamethasone. Indications: For the treatment of infected superficial lesions in dogs caused by bacteria susceptible to gentamicin Limitations: Federal law restricts this drug to use by or on the order of a licensed veterinarian. |
GB Topical Spray
September 5th, 2011
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Flunazine
September 5th, 2011
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ANADA Number: 200-387 |
|
| Proprietary Name |
Flunazine™ |
|---|---|
| Sponsor |
Cross Vetpharm Group Ltd. |
| Sponsor Address |
Broomhill rd. Tallaght, Dublin, 24 |
| Ingredients |
Flunixin Meglumine |
| Species |
Horse, not for meat production Cattle, beef Cattle, dairy, heifers not lactating Cattle, calves, excluding veal calves |
| Routes of Administration |
Intravenous Intramuscular (horse) |
| 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. |
|
Dosage Amount, Indications & Limitations |
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 visceral pain associated with colic. Limitations: Do not use in horses intended for human consumption. 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. 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 and endotoxemia. Also indicated for control of inflammation in endotoxemia. For control of pyrexia associated with acute bovine mastitis. 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.
|
| 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. |
Levamisole Hydrochloride Soluble Drench Powder
September 5th, 2011
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ANADA Number: 200-386 |
|
| Proprietary Name |
Levamisole Hydrochloride Soluble Drench Powder |
|---|---|
| Sponsor |
Teva Animal Health, Inc. |
| Sponsor Address |
3915 South 48th Street Ter. St. Joseph, MO 64506 |
| Ingredients |
Levamisole Hydrochloride |
| Species |
Cattle, beef Sheep, no use class stated or implied |
| Routes of Administration |
Per Os |
| Dose Form |
Liquid (solution) |
| Drug Form |
Powder |
| Dispensing Status |
OTC |
| Withdrawal Time |
Cattle: 48 hours before slaughter. |
|
Dosage Amount, Indications & Limitations |
520.1242a Levamisole hydrochloride drench and drinking water. Specifications: 46.8 grams per packet. Conditions of use: Cattle Amount: 8 milligrams per kilogram body weight as a drench. Indications: Effective against the following adult nematode infections: Stomach worms (Haemonchus placei, Ostertagia ostertagi, Trichostrongylus axei); intestinal worms (T. longispicularis, Cooperia oncophora, C. punctata, Nematodirus spathiger, Bunostomum phlebotomum, Oesophagostomum radiatum); and lungworms (Dictyocaulus viviparus). Limitations: Do not slaughter for food within 48 hours of treatment. Not for use in dairy animals of breeding age. Conditions of constant helminth exposure may require retreatment 2 to 4 weeks after the first treatment. Consult your veterinarian before using in severely debilitated animals. Specifications: 11.7 grams per packet. Sheep Amount: 8 milligrams per kilogram body weight as a drench. Indications: Effective against the following adult nematode infections: Stomach worms (Haemonchus contortus, Trichostrongylus axei, Teladorsagia circumcincta); intestinal worms (Trichostrongylus colubriformis, Cooperia curticei, Nematodirus spathiger, Bunostomum trigonocephalum, Oesophagostomum columbianum, Chabertia ovina), and lungworms (Dictyocaulus filaria). Limitations: Do not slaughter for food within 72 hours of treatment. Conditions of constant helminth exposure may require retreatment 2 to 4 weeks after the first treatment. Consult veterinarian before using in severely debilitated animals. |
| Tolerances |
A tolerance of 0.1 part per million is established for negligible residues of levamisole hydrochloride in the edible tissues of cattle, sheep, and swine. |
ClindaRobe Capsules
September 5th, 2011
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ANADA Number: 200-383 |
|
| Proprietary Name |
ClindaRobe™ Capsules |
|---|---|
| Sponsor |
Novopharm Ltd. |
| Sponsor Address |
30 Novopharm Ct. Toronto, ONT M1B 2K9 |
| Ingredients |
Clindamycin Hydrochloride |
| Species |
Dog, no use class stated or implied |
| Routes of Administration |
Per Os |
| Dose Form |
Capsule |
| Drug Form |
Capsule |
| Dispensing Status |
RX |
| Withdrawal Time |
Withdrawal times do not apply to the species listed for this product. |
|
Dosage Amount, Indications & Limitations |
520.446 Clindamycin hydrochloride capsules. Specifications: Each capsule contains the equivalent of 25, 75, 150 or milligrams of clindamycin as the hydrochloride salt. Conditions of use: Dogs Amount: Wounds, abscesses, and dental infections: 2.5 to 15 milligrams per pound of body weight every 12 hours for a maximum of 28 days. Osteomyelitis: 5.0 to 15 milligrams per poundof body weight every 12 hours for a minimum of 28 days. Indications: For the treatment of skin infections (wounds and abscesses) due to susceptible strains of coagulase-positive staphylococci (Staphylococcus aureus or S. intermedius), deep wounds and abscesses due to susceptible strains of Bacteroides fragilis, Prevotella melaninogenicus, Fusobacterium ecrophorum, and Clostridium perfringens, dental infections due to susceptible strains of S. aureus, B. fragilis, P. melaninogenicus, F. necrophorum, and C. perfringens, and osteomyelitis due to susceptible strains of S. aureus, B. fragilis, P. melaninogenicus, F. necrophorum, and C. perfringens. Limitations: Federal law restricts this drug to use by or on the order of a licensed veterinarian. |
SpecLinx 50
September 5th, 2011
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ANADA Number: 200-380 |
|
| Proprietary Name |
SpecLinx-50™ |
|---|---|
| Sponsor |
Cross Vetpharm Group Ltd. |
| Sponsor Address |
Broomhill rd. Tallaght, Dublin, 24 |
| Ingredients |
Lincomycin Hydrochloride Monohydrate Spectinomycin dihydrochloride pentahydrate |
| Species |
Chicken, up to 7 days old |
| Routes of Administration |
Per Os |
| Dose Form |
Powder |
| Drug Form |
Powder |
| Dispensing Status |
OTC |
| Withdrawal Time |
None established. |
|
Dosage Amount, Indications & Limitations |
520.1265 Lincomycin and spectinomycin soluble powder. Specifications: The following salts of lincomycin and spectinomycin are present in a soluble powder in the ratio of 1 to 2 on the basis of equivalency of lincomycin base to equivalency of spectinomycin base: (1) Lincomycin hydrochloride monohydrate and spectinomycin sulfate tetrahydrate. (2) Lincomycin hydrochloride monohydrate and spectinomycin dihydrochloride pentahydrate. Conditions of use: Chickens for the first 5 to 7 days of life. Amount: 2 grams of antibiotic activity per gallon of drinking water; administer as the sole source of water. Indications: As an aid in the control of airsacculitis caused by either Mycoplasma synoviae or M. gallisepticum susceptible to lincomycin-spectinomycin and complicated chronic respiratory disease (air sac infection) caused by Escherichia coli and M. gallisepticum susceptible to lincomycin-spectinomycin. |
| Tolerances |
A tolerance for residues of lincomycin in chickens is not required. Tolerances for lincomycin in swine of 0.6 part per million in liver and 0.1 part per million in muscle are established. |
Neomycin Liquid
September 5th, 2011
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ANADA Number: 200-379 |
|
| Proprietary Name |
Neomycin Liquid |
|---|---|
| Sponsor |
Sparhawk Laboratories, Inc. |
| Sponsor Address |
12340 Santa Fe Trail Drive Lenexa, KS 66215 |
| Ingredients |
Neomycin Sulfate |
| Species |
Cattle, excluding veal calves Goat, no use class stated or implied Sheep, no use class stated or implied Swine, no use class stated or implied |
| Routes of Administration |
Per Os |
| Dose Form |
Liquid (solution) |
| Drug Form |
Liquid (solution) |
| Dispensing Status |
OTC |
| Withdrawal Time |
Cattle: 1 day before slaughter. |
|
Dosage Amount, Indications & Limitations |
520.1485 Neomycin sulfate oral solution. Specifications: Each milliliter contains 200 milligrams of neomycin sulfate (equivalent to 140 milligrams of neomycin base). Conditions of use: Cattle (excluding veal calves) Amount: 10 milligrams of neomycin sulfate per pound of body weight per day in divided doses for a maximum of 14 days. Indications: For the treatment and control of colibacillosis (bacterial enteritis) caused by Escherichia coli susceptible to neomycin. Limitations: Administer undiluted or in drinking water. Prepare a fresh solution daily. If symptoms persist after using this preparation for 2 or 3 days, consult a veterinarian. Treatment should continue 24 to 48 hours beyond remission of disease symptoms, but not to exceed a total of 14 consecutive days. Discontinue treatment 1 day prior to slaughter. Swine Amount: 10 milligrams of neomycin sulfate per pound of body weight per day in divided doses for a maximum of 14 days. Indications: For the treatment and control of colibacillosis (bacterial enteritis) caused by Escherichia coli susceptible to neomycin. Limitations: Administer undiluted or in drinking water. Prepare a fresh solution daily. If symptoms persist after using this preparation for 2 or 3 days, consult a veterinarian. Treatment should continue 24 to 48 hours beyond remission of disease symptoms, but not to exceed a total of 14 consecutive days. Discontinue treatment 3 days prior to slaughter. Sheep Amount: 10 milligrams of neomycin sulfate per pound of body weight per day in divided doses for a maximum of 14 days. Indications: For the treatment and control of colibacillosis (bacterial enteritis) caused by Escherichia coli susceptible to neomycin. Limitations: Administer undiluted or in drinking water. Prepare a fresh solution daily. If symptoms persist after using this preparation for 2 or 3 days, consult a veterinarian. Treatment should continue 24 to 48 hours beyond remission of disease symptoms, but not to exceed a total of 14 consecutive days. Discontinue treatment 2 days prior to slaughter. Goats Amount: 10 milligrams of neomycin sulfate per pound of body weight per day in divided doses for a maximum of 14 days. Indications: For the treatment and control of colibacillosis (bacterial enteritis) caused by Escherichia coli susceptible to neomycin. Limitations: Administer undiluted or in drinking water. Prepare a fresh solution daily. If symptoms persist after using this preparation for 2 or 3 days, consult a veterinarian. Treatment should continue 24 to 48 hours beyond remission of disease symptoms, but not to exceed a total of 14 consecutive days. Discontinue treatment 3 days prior to slaughter. |
| Tolerances |
Tolerances are established for residues of parent neomycin in uncooked edible tissues as follows: a. In cattle, swine, sheep, and goats: 7.2 parts per million in kidney (target tissue) and fat, 3.6 ppm in liver, and 1.2 ppm in muscle. b. In turkeys: 7.2 ppm in skin with adhering fat, 3.6 parts per million in liver, and 1.2 ppm in muscle. c. In milk: 0.15 part per million. |
Neomycin Sulfate 325
September 5th, 2011
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ANADA Number: 200-378 |
|
| Proprietary Name |
Neomycin Sulfate 325 |
|---|---|
| Sponsor |
Sparhawk Laboratories, Inc. |
| Sponsor Address |
12340 Santa Fe Trail Drive Lenexa, KS 66215 |
| Ingredients |
Neomycin Sulfate |
| Species |
Cattle, excluding veal calves Turkey, growing Goat, no use class stated or implied Sheep, no use class stated or implied Swine, no use class stated or implied |
| Routes of Administration |
Per Os |
| Dose Form |
Liquid (solution) |
| Drug Form |
Powder |
| Dispensing Status |
OTC |
| Withdrawal Time |
Cattle excluding veal calves: 1 day before slaughter |
|
Dosage Amount, Indications & Limitations |
520.1484 Neomycin sulfate soluble powder. Specifications: Each ounce of powder contains 20.3 grams (g) neomycin sulfate (equivalent to 14.2 g neomycin base). Conditions of use: Cattle (excluding veal calves) Amount: 10 milligrams of neomycin sulfate per pound of body weight per day (22 milligrams per kilogram) in divided doses for a maximum of 14 days. Indications: For the treatment and control of colibacillosis (bacterial enteritis) caused by Escherichia coli susceptible to neomycin sulfate. Limitations: Add to drinking water or milk; not for use in liquid supplements. Administer solution undiluted or in drinking water. Prepare a fresh solution daily. If symptoms persist after using this preparation for 2 or 3 days, consult a veterinarian. Treatment should continue 24-48 hours beyond remission of disease symptoms, but not to exceed a total of 14 consecutive days. Discontinue treatment 1 day prior to slaughter in cattle (not for use in veal calves). Swine Amount: 10 milligrams of neomycin sulfate per pound of body weight per day (22 milligrams per kilogram) in divided doses for a maximum of 14 days. Indications: For the treatment and control of colibacillosis (bacterial enteritis) caused by Escherichia coli susceptible to neomycin sulfate. Limitations: Add to drinking water or milk; not for use in liquid supplements. Administer solution undiluted or in drinking water. Prepare a fresh solution daily. If symptoms persist after using this preparation for 2 or 3 days, consult a veterinarian. Treatment should continue 24-48 hours beyond remission of disease symptoms, but not to exceed a total of 14 consecutive days. Discontinue treatment 3 days prior to slaughter in swine. Sheep Amount: 10 milligrams of neomycin sulfate per pound of body weight per day (22 milligrams per kilogram) in divided doses for a maximum of 14 days. Indications: For the treatment and control of colibacillosis (bacterial enteritis) caused by Escherichia coli susceptible to neomycin sulfate. Limitations: Add to drinking water or milk; not for use in liquid supplements. Administer solution undiluted or in drinking water. Prepare a fresh solution daily. If symptoms persist after using this preparation for 2 or 3 days, consult a veterinarian. Treatment should continue 24-48 hours beyond remission of disease symptoms, but not to exceed a total of 14 consecutive days. Discontinue treatment 2 days prior to slaughter in sheep. Goats Amount: 10 milligrams of neomycin sulfate per pound of body weight per day (22 milligrams per kilogram) in divided doses for a maximum of 14 days. Indications: For the treatment and control of colibacillosis (bacterial enteritis) caused by Escherichia coli susceptible to neomycin sulfate. Limitations: Add to drinking water or milk; not for use in liquid supplements. Administer solution undiluted or in drinking water. Prepare a fresh solution daily. If symptoms persist after using this preparation for 2 or 3 days, consult a veterinarian. Treatment should continue 24-48 hours beyond remission of disease symptoms, but not to exceed a total of 14 consecutive days. Discontinue treatment 3 days prior to slaughter in goats. Turkeys (growing) Amount: 10 milligrams of neomycin sulfate per pound of body weight per day (22 milligrams per kilogram) for 5 days. Indications: For the control of mortality associated with E. coli susceptible to neomycin sulfate in growing turkeys. Limitations: Add to drinking water; not for use in liquid supplements. Prepare a fresh solution daily. If symptoms persist after using this preparation for 2 or 3 days, consult a veterinarian. Treatment should continue 24 to 48 hours beyond remission of disease symptoms, but not to exceed a total of 5 consecutive days. |
| Tolerances |
Tolerances are established for residues of parent neomycin in uncooked edible tissues as follows: a. In cattle, swine, sheep, and goats: 7.2 parts per million in kidney (target tissue) and fat, 3.6 ppm in liver, and 1.2 ppm in muscle. b. In turkeys: 7.2 ppm in skin with adhering fat, 3.6 parts per million in liver, and 1.2 ppm in muscle. c. In milk: 0.15 part per million. |
LinxMed SP
September 5th, 2011
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ANADA Number: 200-377 |
|
| Proprietary Name |
LinxMed-SP® |
|---|---|
| Sponsor |
Cross Vetpharm Group Ltd. |
| Sponsor Address |
Broomhill rd. Tallaght, Dublin, 24 |
| Ingredients |
Lincomycin Hydrochloride |
| Species |
Chicken, broilers excluding layers and breeders Swine, no use class stated or implied |
| Routes of Administration |
Per Os |
| Dose Form |
Liquid (solution) |
| Drug Form |
Powder |
| Dispensing Status |
OTC |
| Withdrawal Time |
Swine: zero days before slaughter. |
|
Dosage Amount, Indications & Limitations |
520.1263c Lincomycin hydrochloride soluble powder. Specifications: Each gram of soluble powder contains lincomycin hydrochloride equivalent to 0.4 grams of lincomycin. Conditions of use: Swine Amount: 250 milligrams per gallon of drinking water to provide 3.8 milligrams per pound of body weight per day. Indications: For the treatment of swine dysentery (bloody scours). Limitations: Discard medicated drinking water if not used within 2 days. Prepare fresh stock solution daily. Do not use for more than 10 days. If clinical signs of disease have not improved within 6 days, discontinue treatment and reevaluate diagnosis. The safety of lincomycin has not been demonstrated in pregnant swine or swine intended for breeding. Chickens: Amount. 64 milligrams per gallon of drinking water. Indications: For the control of necrotic enteritis caused by Clostridium perfringens susceptible to lincomycin in broiler chickens. Limitations: Discard medicated drinking water if not used within 2 days. Prepare fresh stock solution daily. Administer for 7 consecutive days. Do not allow rabbits, hamsters, guinea pigs, horses, or ruminants access to water containing lincomycin. Not for use in layer and breeder chickens. |
| Tolerances |
A tolerance for residues of lincomycin in chickens is not required. Tolerances for lincomycin in swine of 0.6 part per million in liver and 0.1 part per million in muscle are established. |
Sulfamed G
September 5th, 2011
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ANADA Number: 200-376 |
|
| Proprietary Name |
Sulfamed-G™ |
|---|---|
| Sponsor |
Cross Vetpharm Group Ltd. |
| Sponsor Address |
Broomhill rd. Tallaght, Dublin, 24 |
| Ingredients |
Sulfadimethoxine |
| Species |
Cattle, beef Cattle, dairy, heifers Cattle, dairy, calves Turkey, meat type, up to 24 weeks age Chicken, replacements Chicken, broilers |
| Routes of Administration |
Per Os |
| Dose Form |
Liquid (solution) |
| Drug Form |
Powder |
| Dispensing Status |
OTC |
| Withdrawal Time |
Cattle: 7 days before slaughter |
|
Dosage Amount, Indications & Limitations |
520.2220a Sulfadimethoxine oral solution and soluble powder. Specifications: Each packet of powder contains the equivalent of 94.6 grams of sulfadimethoxine (as the sodium salt). Conditions of use: Chickens (broilers and replacements) Amount: 1.875 (0.05 percent) grams of powder per gallon to prepare a drench or drinking water. Indications: Treatment of disease outbreaks of coccidiosis, fowl cholera, and infectious coryza. Limitations: Administer for 6 consecutive days. Do not administer to chickens over 16 weeks of age. As sole source of drinking water and sulfonamide medication. As sulfadimethoxine solution or sulfadimethoxine soluble sodium salt. Withdraw 5 days prior to slaughter. Chickens and turkeys that have survived fowl cholera outbreaks should not be kept for replacements or breeders. Turkeys (meat) Amount: 0.938 (0.025 percent) grams of powder per gallon to prepare a drench or drinking water. Indications: Treatment of disease outbreaks of coccidiosis and fowl cholera. Limitations: Administer for 6 consecutive days. Do not administer to turkeys over 24 weeks of age. As sole source of drinking water and sulfonamide medication. As sulfadimethoxine solution or sulfadimethoxine soluble sodium salt. Withdraw 5 days prior to slaughter. Chickens and turkeys that have survived fowl cholera outbreaks should not be kept for replacements or breeders. Cattle (dairy calves, dairy heifers, and beef cattle) Amount: 1.18 to 2.36 (0.031 to 0.062 percent) grams of powder per gallon to prepare a drench or drinking water. Administer 2.5 grams per 100 pounds of body weight for first day, then 1.25 grams per 100 pounds of body weight per day for the next 4 consecutive days. In drinking water or drench. Available as a sulfadimethoxine soluble powder or a 12.5 percent sulfadimethoxine sodium solution (3.75 grams sulfadimethoxine per fluid ounce). Indications: Treatment of shipping fever complex, bacterial pneumonia, calf diphtheria, and foot rot. Limitations: If no improvement within 2 to 3 days, reevaluate diagnosis. Do not treat beyond 5 days. Withdraw 7 days prior to slaughter. Federal law prohibits the extralabel use of this product in lactating dairy cattle. A withdrawal period has not been established for this product in preruminating calves. Do not use in calves to be processed for veal. |
| Tolerances |
Tolerances are established for residues of sulfadimethoxine in edible products of animals as follows: a. Chickens, turkeys, cattle, ducks, salmonids, catfish and chukar partridges: 0.1 part per million (negligible residue) in uncooked edible tissues b. Milk: 0.01 part per million (negligible residue). |
HeifermaX 500 Rumensin Tylan
September 5th, 2011
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ANADA Number: 200-375 |
|
| Proprietary Name |
HeifermaX™ 500 / Rumensin® / Tylan® |
|---|---|
| Sponsor |
Ivy Laboratories, Division of Ivy Animal Health, Inc. |
| Sponsor Address |
8857 Bond Street Overland Park, KS 66214 |
| Ingredients |
Melengestrol Acetate Monensin Sodium Tylosin Phosphate |
| Species |
Cattle, beef, heifers fed in confinement for slaughter |
| Routes of Administration |
Per Os |
| Dose Form |
Medicated feed |
| Drug Form |
Type A Medicated Article |
| Dispensing Status |
OTC |
| Withdrawal Time |
Zero withdrawal |
|
Dosage Amount, Indications & Limitations |
558.342 Melengestrol acetate. Specifications: Dry Type A medicated articles containing 100 or 200 milligrams per pound or liquid Type A article containing 500 milligrams per pound Conditions of use: Cattle (heifers fed in confinement for slaughter) Amount: Melengestrol acetate, 0.25 to 0.50 milligram per head per day, plus monensin (as monensin sodium) at 50 to 360 milligrams per head per day, plus tylosin (as tylosin phosphate), 60 to 90 milligrams per head per day. To attain this amount: Add 0.5 to 2.0 pounds per head per day of a liquid or dry medicated feed containing 0.125 to 1.0 milligram of melengestrol acetate per pound to a medicated feed containing 5 to 30 grams of monensin and 8 to 10 grams of tylosin per ton; or Add 0.5 to 2.0 pounds per head per day of a liquid or dry medicated feed containing 0.125 to 1.0 milligram of melengestrol acetate plus 25 to 720 milligrams of monensin per pound to 4.5 to 18 pounds of a dry medicated feed containing 10 to 40 grams of tylosin per ton; or Add 0.5 to 2.0 pounds per head per day of a dry pelleted medicated feed containing 0.125 to 1.0 milligram of melengestrol acetate (from a dry Type A article), 25 to 600 milligrams of monensin, plus 45 to 180 milligrams of tylosin per pound to a ration of non-medicated feed. Indications: For increased rate of weight gain, improved feed efficiency, suppression of estrus (heat), for the prevention and control of coccidiosis due to Eimeria bovis and Eimeria zuernii; and for reduced incidence of liver abscesses caused by Fusobacterium necrophorum and Actinomyces (Corynebacterium) pyogenes. Limitations: For heifers fed in confinement for slaughter. |
| Tolerances |
A tolerance of 0.10 part per million (ppm) in cattle liver, 0.05 ppm in muscle, kidney, and fate. A tolerance of 0.05 ppm in goats edible tissue. A tolerance for residue of monensin in chickens, turkeys and quail is not needed. A tolerance for residues of monensin in milk is not needed. Tolerances are established for residues of tylosin in edible products of animals as follows: a. Chickens and turkeys: 0.2 part per million (negligible residue) in uncooked fat, muscle, liver, and kidney. b. Cattle: 0.2 part per million (negligible residue) in uncooked fat, muscle, liver, and kidney. c. Swine: 0.2 part per million (negligible residue) in uncooked fat, muscle, liver, and kidney. d. Milk: 0.05 part per million (negligible residue). e. Eggs: 0.2 part per million (negligible residue). A tolerance of 25 parts per billion is established for residues of the parent compound, melengestrol acetate, in fat, of cattle. |
