Label: CHLORMAX 50- chlortetracycline granule
- NDC Code(s): 54771-1212-1
- Packager: Zoetis Inc.
- Category: VFD TYPE A MEDICATED ARTICLE ANIMAL DRUG LABEL
- DEA Schedule: None
- Marketing Status: New Animal Drug Application
Drug Label Information
Updated May 12, 2021
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Indications for Use
Indications for use Chlortetracycline mg / lb body wt / day Cattle Beef cattle (over 700 lbs): Control of active infection of anaplasmosis caused by Anaplasma marginale susceptible to chlortetracycline.
Withdraw 48 hours prior to slaughter.
0.5 Calves, beef and non-lactating dairy cattle: Treatment of bacterial enteritis caused by Escherichia coli and bacterial pneumonia caused by Pasteurella multocida organisms susceptible to chlortetracycline.
Treat for not more than 5 days.
Withdraw 24 hours prior to slaughter.10 Swine Control of porcine proliferative enteropathies (ileitis) caused by Lawsonia intracellularis susceptible to chlortetracycline.
Treatment of bacterial enteritis caused by Escherichia coli and Salmonella choleraesuis and bacterial pneumonia caused by Pasteurella multocida organisms susceptible to chlortetracycline. (Note: This drug level is equivalent to 400 grams per ton, depending on feed consumption and body weight).
Feed for not more than 14 days.10 Turkeys Control of complicating bacterial organisms associated with bluecomb (transmissible enteritis, coronaviral enteritis) susceptible to chlortetracycline. Feed continuously for 7 to 14 days. 25 Indications for use mg / head / day Cattle Growing cattle (over 400 lbs): For the reduction of the incidence of liver abscesses. 70 Beef cattle: For the control of bacterial pneumonia associated with shipping fever complex caused by Pasteurella spp. susceptible to chlortetracycline.
Withdraw 48 hours prior to slaughter.
350 Beef cattle (under 700 lbs): Control of active infection of anaplasmosis caused by Anaplasma marginale susceptible to chlortetracycline.
Withdraw 48 hours prior to slaughter.350 Sheep Breeding sheep: Reducing the incidence of (vibrionic) abortion caused by Campylobacter fetus infection susceptible to chlortetracycline. 80 Indications for use In complete feed Chlortetracycline g / ton Chickens Control of infectious synovitis caused by Mycoplasma synoviae susceptible to chlortetracycline. Feed continuously for 7 to 14 days.
100 - 200 Control of chronic respiratory disease (CRD) and air sac infection caused by Mycoplasma gallisepticum and Escherichia coli susceptible to chlortetracycline. Feed continuously for 7 to 14 days.
200 - 400 Reduction of mortality due to Escherichia coli infections susceptible to chlortetracycline.
Feed for 5 days.
Withdraw 24 hours prior to slaughter.500 Turkeys Control of infectious synovitis caused by Mycoplasma synoviae susceptible to chlortetracycline.
Feed continuously for 7 to 14 days.
200 Control of hexamitiasis caused by Hexamita meleagridis susceptible to chlortetracycline. Feed continuously for 7 to 14 days.
400 Turkey poults not over 4 weeks of age: Reduction of mortality due to paratyphoid caused by Salmonella typhimurium susceptible to chlortetracycline. 400 Swine Reducing the incidence of cervical lymphadenitis (jowl abscesses) caused by Group E Streptococci susceptible to chlortetracycline.
50 - 100 Breeding swine: Control of leptospirosis (reducing the incidence of abortion and shedding of leptospirae) caused by Leptospira pomona susceptible to chlortetracycline.
Feed continuously for not more than 14 days.400 -
Mixing directions
For use in manufacture of complete feeds, mix thoroughly as follows:
Chlortetracycline, g/ton ChlorMax 50, lb/ton 50 - 100 1 - 2 100 - 200 2 - 4 200 - 400 4 - 8 500 10 For use in manufacture of feed supplements to be fed at a rate of 1 lb per head per day, mix thoroughly as follows:
mg/lb body wt/day If animal wt = 1000 lbs ChlorMax 50 lb/ton supplement 0.5 500 mg 20 5.0 5,000 mg 200 - Caution
- Warning
- Storage
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- PRINCIPAL DISPLAY PANEL - 22.68 LABEL
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INGREDIENTS AND APPEARANCE
CHLORMAX 50
chlortetracycline granuleProduct Information Product Type VFD TYPE A MEDICATED ARTICLE ANIMAL DRUG Item Code (Source) NDC:54771-1212 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength CHLORTETRACYCLINE (UNII: WCK1KIQ23Q) (CHLORTETRACYCLINE - UNII:WCK1KIQ23Q) CHLORTETRACYCLINE 50 g in 0.45 kg Product Characteristics Color brown (Light Tan to Brown) Score Shape Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:54771-1212-1 22.68 kg in 1 BAG Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date NADA NADA046699 02/15/2016 Labeler - Zoetis Inc. (828851555)