Durvet Pennchlor 50
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Questions & Answers
Side Effects & Adverse Reactions
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Legal Issues
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FDA Safety Alerts
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Manufacturer Warnings
There is currently no manufacturer warning information available for this drug.
FDA Labeling Changes
There are currently no FDA labeling changes available for this drug.
Uses
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lbs. of |
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Use Levels of | Pennchlor 50 |
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Chlortetracycline | per ton |
| Indications for Use | |
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| CHICKENS |
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| For Broiler/fryer chickens: For an increased rate of weight gain and |
10-50 g/ton |
0.2-1.0 |
| improved feed efficiency. |
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| WARNING: Do not feed to chickens producing eggs for human |
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| consumption. Zero-day withdrawal period. |
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| For Chickens: Control of infectious synovitis caused by Mycoplasma | 100-200 g/ton |
2.0-4.0 |
| synoviae susceptible to chlortetracycline. (Feed continuously for 7-14 |
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| days) |
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| WARNING: Do not feed to chickens producing eggs for human |
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| consumption. Zero-day withdrawal period. |
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| For Chickens: Control of chronic respiratory disease (CRD) and air sac |
200-400 g/ton |
4.0-8.0 |
| infections caused by Mycoplasma gallisepticum and Escherichia coli | |
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| susceptible to chlortetracycline. (Feed continuously for 7-14 days) |
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| WARNING: Do not feed to chickens producing eggs for human |
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| consumption. Zero-day withdrawal period. |
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| For Chickens: Reduction of mortality due to Escherichia coli infections |
500 g/ton |
10.0 |
| susceptible to chlortetracycline. (Feed for 5 days) |
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| WARNING: Do not feed to chickens producing eggs for human |
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| consumption. Withdraw 24 hours prior to slaughter. |
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| TURKEYS |
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| For Turkeys: Growing Turkeys: For an increased rate of weight gain |
10-50 g/ton |
0.2-1.0 |
| and improved feed efficiency. |
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| WARNING: Do not feed to turkeys producing eggs for human |
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| consumption. Zero-day withdrawal period. |
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| For Turkeys: Control of infectious synovitis caused by Mycoplasma | 200 g/ton |
4.0 |
| synoviae susceptible to chlortetracycline. (Feed continuously for 7-14 days) |
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| WARNING: Do not feed to turkeys producing eggs for human |
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| consumption. Zero-day withdrawal period. |
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| For Turkeys: Control of hexamitiasis caused by Hexamita meleagrides | 400 g/ton |
8.0 |
| susceptible to chlortetracycline. (Feed continuously 7-14 days) |
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| WARNING: Do not feed to turkeys producing eggs for human |
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| consumption. Zero-day withdrawal period. |
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| |
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| For Turkeys: Turkey poults not over 4 weeks of age: Reduction of |
400 g/ton |
8.0 |
| mortality due to paratyphoid caused by Salmonella typhimurium | |
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| susceptible to chlortetracycline. |
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| For Turkeys: Control of complicating bacterial organisms associated |
25 mg/lb body weight/day |
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| with bluecomb (transmissible enteritis, coronaviral enteritis) susceptible |
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| to chlortetracycline. (Feed continuously for 7-14 days) |
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| WARNING: Do not feed to turkeys producing eggs for human |
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| consumption. Zero-day withdrawal period. |
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| SHEEP | |
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| For Growing Sheep: For an increased rate of weight gain and improved |
20-50 g/ton |
0.4-1.0 |
| feed efficiency. |
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| For Breeding Sheep: Reducing the incidence of (vibrionic) abortion |
80 mg/head/day |
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| caused by Campylobacter fetus infections susceptible to chlortetracycline. |
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| WARNING: Zero-day withdrawal period. |
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| |
|
lbs. of |
| |
Use Levels of | Pennchlor 50 |
| |
Chlortetracycline |
per ton |
| Indications for Use | |
|
| |
|
|
| SWINE | |
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| For Growing Swine: For an increased rate of weight gain | 10-50 g/ton |
0.2-1.0 |
| improved feed efficiency. |
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| |
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| For Swine: Reducing the incidence of cervical lymphadenitis |
50-100 g/ton |
1.0-2.0 |
| (jowl abscesses) caused by Group E Streptococci susceptible to |
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| chlortetracycline. |
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| For Breeding Swine: Control of leptospirosis (reducing the instances |
400 g/ton |
8.0 |
| of abortions and shedding of leptospirae) caused by Leptospira pomona | |
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| susceptible to chlortetracycline. (Feed continuously for 14 days) |
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| For Swine: Treatment of bacterial enteritis caused by Escherichia coli | Feed approximately 400 g/t, |
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| and Salmonella choleraesius and bacterial pneumonia caused by |
varying with body weight and |
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| Pasteurella multocida susceptible to chlortetracycline. (Feed for not |
feed consumption to provide |
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| more than 14 days) |
10 mg/lb body weight/day |
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| WARNING: Zero-day withdrawal period. |
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| CALVES, BEEF CATTLE, AND NONLACTATING DAIRY CATTLE | |
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| WARNING: A WITHDRAWAL PERIOD HAS NOT BEEN ESTABLISHED |
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| FOR THIS PRODUCT IN PRE-RUMINATING CALVES. DO NOT USE |
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| IN CALVES TO BE PROCESSED FOR VEAL. |
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| For Calves (up to 250 lbs.): For an increased rate of weight gain and |
0.1 mg/lb body weight/day |
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| improved feed efficiency. |
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| For Calves (250-400 lbs.): For an increased rate of weight gain and |
25-70 mg/head/day |
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| improved feed efficiency. |
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| For Growing Cattle (over 400 lbs.): For an increased rate of weight |
70 mg/head/day |
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| gain, improved feed efficiency and reduction of liver condemnation |
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| due to liver abscesses. |
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| For Beef Cattle: For the control of bacterial pneumonia associated with |
350 mg/head/day |
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| shipping fever complex caused by Pasteurella spp. susceptible to |
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| chlortetracycline. |
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| WARNING: Zero-day withdrawal period. |
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| For Beef Cattle (under 700 lbs.): Control of active infection of anaplasmosis |
350 mg/head/day |
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| caused by Anaplasma marginale susceptible to chlortetracycline. |
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| WARNING: Zero-day withdrawal period. |
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| For Beef Cattle (over 700 lbs.): Control of active infection of |
0.5 mg/lb body weight/day |
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| anaplasmosis caused by Anaplasma marginale susceptible to |
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| chlortetraycline. |
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| WARNING: Zero-day withdrawal period |
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| For Calves, Beef, and Nonlactating Dairy Cattle: For treatment of |
10 mg/lb body weight/day |
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| bacterial enteritis caused by Escherichia coli and bacterial pneumonia |
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| caused by Pasteurella multocida susceptible to chlortetracycline. |
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| (Treat for not more than 5 days) |
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| WARNING: Zero-day withdrawal period. |
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History
There is currently no drug history available for this drug.
Other Information
There are no additional details available for this product.
Sources
Durvet Pennchlor 50 Manufacturers
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Durvet, Inc.
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Durvet Pennchlor 50 | Durvet, Inc.
There is currently no dosage information available for this product. We apologize for any inconvenience.
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