Panacur

Generic Name: fenbendazole suspension
Dosage Form: FOR ANIMAL USE ONLY

intervet
Panacur®
(fenbendazole)
Dewormer for Beef & Dairy Cattle

Suspension 10% (100 mg/mL)

DOSAGE

Beef and Dairy Cattle

5 mg/kg (2.3 mg/lb) for the removal and control of:

Lungworm: (Dictyocaulus viviparus)

Stomach worm (adults): Ostertagia ostertagi (brown stomach worm).

Stomach worm (adults & 4th stage larvae): Haemonchus contortus/placei (barberpole worm), Trichostrongylus axei (small stomach worm).

Intestinal worm (adults & 4th stage larvae): Bunostomum phlebotomum (hookworm), Nematodirus helvetianus (threadnecked intestinal worm), Cooperia punctata and C. oncophora (small intestinal worm), Trichostrongylus colubriformis (bankrupt worm), Oesophagostomum radiatum (nodular worm).

Beef Cattle Only

10 mg/kg (4.6 mg/lb) for the removal and control of:

Stomach worm (4th stage inhibited larvae): Ostertagia ostertagi (Type II Ostertagiasis)

Tapeworm: Moniezia benedeni

Do not use in dairy cattle at 10 mg/kg.

DIRECTIONS

Determine the proper dose according to estimated body weight. Administer orally. In beef and dairy cattle, the recommended dose of 5 mg/kg is achieved when 2.3 mL of the drug are given for each 100 lb of body weight. In beef cattle only, the recommended dosage of 10 mg/kg for treatment of Ostertagiasis Type II (inhibited 4th stage larvae) or tapeworm is achieved when 4.6 mL of the drug is given for each 100 lb of body weight.

EXAMPLES: Dose
(5 mg/kg)
Dose
(10 mg/kg)
Cattle
Weight
  2.3 mL   4.6 mL 100 lb
  4.6 mL   9.2 mL 200 lb
  6.9 mL 13.8 mL 300 lb
  9.2 mL 18.4 mL 400 lb
11.5 mL 23.0 mL 500 lb
23.0 mL 46.0 mL 1,000 lb    
34.5 mL 69.0 mL 1,500 lb    

Under conditions of continued exposure to parasites, retreatment may be needed after 4-6 weeks. There are no known contraindications to the use of the drug in cattle. For dairy cattle, there is no milk withdrawal period at 5 mg/kg.

Store at or below 25°C (77°F).

Protect from freezing.

Shake well before use.

RESIDUE WARNINGS

Cattle must not be slaughtered for human consumption within 8 days following treatment. For dairy cattle, there is no milk withdrawal period at the 5 mg/kg dose. Do not use at 10 mg/kg in dairy cattle. Dose rate of 10 mg/kg is for beef cattle only. Dose rate of 10 mg/kg in dairy cattle could result in violative residues in milk. A withdrawal period has not been established for this product in pre-ruminating calves. Do not use in calves to be processed for veal.

CAUTION

Federal law restricts this drug to use by or on the order of a licensed veterinarian.

Keep this and all medication out of the reach of children.

Made in France
Distributed by: Intervet Inc., Millsboro, DE 19966

NADA # 128-620, Approved by FDA

PRINCIPAL DISPLAY PANEL - 3,785 mL Label

intervet

Panacur®
(fenbendazole)

Dewormer for Beef & Dairy Cattle Suspension 10% (100 mg/mL)

RESIDUE WARNINGS: Cattle must not be slaughtered for human
consumption within 8 days following treatment. For dairy cattle,
there is no milk withdrawal period at the 5 mg/kg dose. Do not use
at 10 mg/kg in dairy cattle. Dose rate of 10 mg/kg is for beef cattle
only. Dose rate of 10 mg/kg in dairy cattle could result in violative
residues in milk. A withdrawal period has not been established for
this product in pre-ruminating calves. Do not use in calves to be
processed for veal.

CAUTION: Federal law restricts this drug to use
by or on the order of a licensed veterinarian.

Keep this and all medication out of the
reach of children.

1 Gallon (3,785 mL)

055602 LPFI240 01

Panacur 
fenbendazole suspension
Product Information
Product Type PRESCRIPTION ANIMAL DRUG Item Code (Source) NDC:57926-086
Route of Administration ORAL DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
Fenbendazole (Fenbendazole) Fenbendazole 100 mg  in 1 mL
Inactive Ingredients
Ingredient Name Strength
methylparaben  
propylparaben  
silicon dioxide  
carboxymethylcellulose sodium  
povidone  
trisodium citrate dihydrate  
citric acid monohydrate  
water  
Packaging
# Item Code Package Description
1 NDC:57926-086-01 3785 mL in 1 BOTTLE
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
NADA NADA128620 09/16/2009
Labeler - Schering Corporation (001317601)
Establishment
Name Address ID/FEI Operations
Intervet Production S.A. 771867553 ANALYSIS, MANUFACTURE
Revised: 09/2009
 
Schering Corporation



Hide
(web5)