Monday, September 19, 2016

Program 6 Month Injectable





Dosage Form: FOR ANIMAL USE ONLY
Program 6 Month Injectable for Cats

6 Month Injectable for Cats


The six-month injection that controls flea populations in cats.



Caution


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



Description


PROGRAM® (lufenuron) 6 Month Injectable for Cats is available in two syringe sizes for subcutaneous administration to cats and kittens according to their weight (See Dosage). Each preloaded syringe is formulated to provide 4.54 mg/pound (10 mg/kg) body weight of lufenuron. The active ingredient of Program 6 Month Injectable for Cats is lufenuron, a benzoylphenyl-urea derivative with the following chemical composition: N-[2,5-dichloro-4-(1,1,2,3,3,3,-hexafluoropropoxy)-phenylaminocarbonyl]-2,6-difluorobenzamide. Benzoylphenyl-urea compounds, including lufenuron, are classified as insect development inhibitors (IDIs).



Mode of Action


Lufenuron, the active ingredient of Program 6 Month Injectable for Cats, is an insect development inhibitor which breaks the flea life cycle by inhibiting egg development. Lufenuron’s mode of action is interference with chitin synthesis, polymerization and deposition. Lufenuron has no effect on adult fleas.


After biting a lufenuron-treated cat, the female flea ingests a blood meal containing lufenuron which is subsequently deposited in her eggs. Lufenuron prevents flea eggs from hatching and developing into adults and thus controls flea populations by breaking the life cycle. (See Efficacy.)



Indications


Program 6 Month Injectable for Cats is indicated for use in cats, six weeks of age and older, for the control of flea populations.


Lufenuron controls flea populations by preventing the development of flea eggs and does not kill adult fleas. Concurrent use of insecticides may be necessary for adequate control of adult fleas.



Warning


Do not use in dogs. A severe local reaction may occur in dogs that is not seen in cats.



Precautions


The safety of Program 6 Month Injectable for Cats in reproducing animals has not been established.


Program 6 Month Injectable for Cats breaks the flea life cycle by inhibiting egg development. However, pre-existing flea populations may continue to develop and emerge after treatment with Program 6 Month Injectable for Cats. Based on results of clinical studies, this emergence generally occurs during the first 30-60 days. Therefore, noticeable control may not be observed until several weeks after dosing when a pre-existing infestation is present. Cooler geographic areas may have longer lag periods due to a prolonged flea life cycle. Insecticides may be used concurrently depending on the severity of the infestation.



Efficacy


Laboratory and clinical trials have shown that Program 6 Month Injectable for Cats is a safe, effective and convenient method to control flea populations. A single dose provides long-lasting control for a full 6 months.


In laboratory studies, Program 6 Month Injectable for Cats provided a cumulative percent control of egg development of 94.8% and 97.7% beginning 14 days post-treatment through six months post-treatment in the dose titration and dose confirmation studies, respectively. There was a 2-3 week “induction phase” in these studies before significant effects on flea reproduction were seen.


Program 6 Month Injectable for Cats was effective in controlling flea populations when administered to 183 pet cats in a clinical setting. At study initiation, treated cats averaged 43 fleas per cat. Six months post-injection these cats averaged 11 fleas per cat.



Safety


Program 6 Month Injectable for Cats has been used and tested safely in over sixteen breeds of cats, including females, males and kittens. In well-controlled clinical trials, 294 cats were treated with lufenuron. Program 6 Month Injectable for Cats has also been safely used in cats receiving frequently used veterinary products such as vaccines, anthelmintics, antibiotics, steroids and insecticides.


The acute toxicity of injectable lufenuron was evaluated by administering 100 mg/kg bw, 10x the recommended 10 mg/kg bw dose rate, to adult cats. The potential cumulative toxicity of 1x and 3x the 10 mg/kg six month use rate of lufenuron injectable in 2 week old kittens was evaluated over a two month period. Other than injection site reactions (see below), no clinical signs of toxicity were reported in these studies.


Cumulative toxicity of injectable lufenuron in 2 month old cats was evaluated by administering 1, 3, or 5x the six-month dose three times during the 6 month study. This equates to cumulative doses of 3X, 9X, and 15X, respectively. Other than injection site reactions (see below), no clinical signs of toxicity were reported in these studies. Heinz body inclusions were present in all the control and treated cats, however, erythrocytes in the 50 mg/kg (15x cumulative dose) group had slightly elevated levels of Heinz bodies at 3-6 months.


The following injection site reactions were noted in these laboratory studies. Transient, minor discomfort was noted in some kittens and cats upon injection. Small raised areas at the injection sites, presumed to be deposits of lufenuron, were seen immediately after administration and persisted in some cases for the duration of the studies.This response at the injection site correlated microscopically with acute to granulomatous inflammation and fibrosis. Older injection sites showed less inflammation which indicates these effects may resolve with time. No neoplastic transformations were found. (See Adverse Reactions.)



Dosage


Program 6 Month Injectable for Cats is injected subcutaneously once every six months at the recommended minimum dosage of 4.54 mg lufenuron per pound (10 mg/kg) of body weight. 



Recommended Dosage Schedule                       











Body WeightSyringe SizeLufenuron Dose
Up to 8.8 lbs. (4.0 kg)
Small (0.4 ml)40 mg
8.9 lbs. to 17.6 lbs. (4.1 to 8.0 kg)Large (0.8 ml)80 mg

Administration


Administer Program 6 Month Injectable for Cats subcutaneously using standard injection technique. Before administration, shake well to thoroughly mix the sterile suspension. Remove the needle guard and subcutaneously inject the entire contents of the syringe. Do not inject intramuscularly. The empty syringe should be disposed of in an approved manner.


To ensure the greatest benefits from the use of Program 6 Month Injectable for Cats, it is important to treat all cats within a household. All dogs within the household should be treated with lufenuron tablets. Untreated dogs and cats may develop infestations which could reduce the overall flea control within a household.


Do not administer this product to dogs.



Adverse Reactions


The following adverse reactions were observed in clinical field trials with Program 6 Month Injectable for Cats: pain on injection, injection site lumps/granulomas, vomiting, listlessness/lethargy and anorexia.


Histologic examination of one cat’s injection site lump showed evidence of inflammation surrounding an area of necrosis with marked proliferation of fibrous connective tissue. In another cat, granulamatous inflammation was noted which included non-pleomorphic fibrocytes and fibroplasia.



How Supplied


Program 6 Month Injectable for Cats is available in 0.4 ml and 0.8 ml unit dose syringes, formulated according to the weight of the cat. Unit dose packs are available in packages of 10 syringes per carton.



Storage Conditions


Program 6 Month Injectable for Cats should be stored at room temperature between 59° and 86 °F (15-30 °C).


NADA# 141-105, Approved by FDA


Manufactured for:


Novartis Animal Health US, Inc.,


Greensboro, NC 27404


© 1998 Novartis


NAH/PRO-FI/VI/1 


2/98



PRINCIPAL DISPLAY PANEL


Package Label – 40 mg


FOR CAT


TREATMENT ONLY


NOVARTIS


PROGRAM® (LUFENURON) 6 MONTH INJECTABLE FOR CATS 


40 mg.


up to 8.8 lbs.


Net Contents: Each syringe contains


40 mg LUFENURON in 0.4 mL


Contents: 10 syringes


Product #50911


NADA# 141-105, Approved by FDA


Caution: Federal (USA) law restricts this drug


to be used by the order of a licensed veterinarian.


Keep this and all drugs out


of the reach of children




PRINCIPAL DISPLAY PANEL


Package Label – 80 mg


FOR CAT


TREATMENT ONLY


NOVARTIS


PROGRAM® (LUFENURON) 6 MONTH INJECTABLE FOR CATS 


80 mg.


8.9 to 17.6 lbs.


Net Contents: Each syringe contains


80 mg LUFENURON in 0.8 mL


Contents: 10 syringes


Product #50921


NADA# 141-105, Approved by FDA


Caution: Federal (USA) law restricts this drug


to be used by the order of a licensed veterinarian.


Keep this and all drugs out


of the reach of children










Program 6 Month Injectable FOR CATS 
lufenuron  injection, suspension










Product Information
Product TypePRESCRIPTION ANIMAL DRUGNDC Product Code (Source)58198-5091
Route of AdministrationSUBCUTANEOUSDEA Schedule    








Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
LUFENURON (LUFENURON)LUFENURON100 mg  in 1 mL





Inactive Ingredients
Ingredient NameStrength
No Inactive Ingredients Found


















Product Characteristics
Color    Score    
ShapeSize
FlavorImprint Code
Contains      














Packaging
#NDCPackage DescriptionMultilevel Packaging
158198-5091-110 SYRINGE In 1 CARTONcontains a SYRINGE, PLASTIC
10.4 mL In 1 SYRINGE, PLASTICThis package is contained within the CARTON (58198-5091-1)










Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
NADANADA14110503/13/1998







Program 6 Month Injectable FOR CATS 
lufenuron  injection, suspension










Product Information
Product TypePRESCRIPTION ANIMAL DRUGNDC Product Code (Source)58198-5092
Route of AdministrationSUBCUTANEOUSDEA Schedule    








Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
LUFENURON (LUFENURON)LUFENURON100 mg  in 1 mL





Inactive Ingredients
Ingredient NameStrength
No Inactive Ingredients Found


















Product Characteristics
Color    Score    
ShapeSize
FlavorImprint Code
Contains      














Packaging
#NDCPackage DescriptionMultilevel Packaging
158198-5092-110 SYRINGE In 1 CARTONcontains a SYRINGE, PLASTIC
10.8 mL In 1 SYRINGE, PLASTICThis package is contained within the CARTON (58198-5092-1)










Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
NADANADA14110503/13/1998


Labeler - Novartis Animal Health US, Inc. (966985624)
Revised: 03/1998Novartis Animal Health US, Inc.

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