Tuesday 28 September 2010

Nor Sartan




Nor Sartan may be available in the countries listed below.


Ingredient matches for Nor Sartan



Losartan

Losartan potassium salt (a derivative of Losartan) is reported as an ingredient of Nor Sartan in the following countries:


  • Dominican Republic

  • El Salvador

  • Guatemala

  • Honduras

  • Nicaragua

  • Panama

International Drug Name Search

Ciprofloxacin Aurus




Ciprofloxacin Aurus may be available in the countries listed below.


Ingredient matches for Ciprofloxacin Aurus



Ciprofloxacin

Ciprofloxacin hydrochloride (a derivative of Ciprofloxacin) is reported as an ingredient of Ciprofloxacin Aurus in the following countries:


  • Germany

International Drug Name Search

Saturday 25 September 2010

Prosek




Prosek may be available in the countries listed below.


Ingredient matches for Prosek



Omeprazole

Omeprazole is reported as an ingredient of Prosek in the following countries:


  • Turkey

International Drug Name Search

Monday 20 September 2010

Artelac Advanced MDO




Artelac Advanced MDO may be available in the countries listed below.


Ingredient matches for Artelac Advanced MDO



Hyaluronic Acid

Hyaluronic Acid is reported as an ingredient of Artelac Advanced MDO in the following countries:


  • Germany

International Drug Name Search

Fludocel




Fludocel may be available in the countries listed below.


Ingredient matches for Fludocel



Fluconazole

Fluconazole is reported as an ingredient of Fludocel in the following countries:


  • Portugal

International Drug Name Search

Sunday 19 September 2010

Zelapar




In the US, Zelapar (selegiline systemic) is a member of the following drug classes: dopaminergic antiparkinsonism agents, monoamine oxidase inhibitors and is used to treat ADHD, Depression and Parkinson's Disease.

US matches:

  • Zelapar

  • Zelapar Orally Disintegrating Tablets

UK matches:

  • Zelapar
  • Zelapar (Cephalon Limited) (SPC)

Ingredient matches for Zelapar



Selegiline

Selegiline hydrochloride (a derivative of Selegiline) is reported as an ingredient of Zelapar in the following countries:


  • Argentina

  • United Kingdom

  • United States

International Drug Name Search

Glossary

SPC Summary of Product Characteristics (UK)

Click for further information on drug naming conventions and International Nonproprietary Names.

Wednesday 15 September 2010

Zesger




Zesger may be available in the countries listed below.


Ingredient matches for Zesger



Lisinopril

Lisinopril is reported as an ingredient of Zesger in the following countries:


  • Ireland

International Drug Name Search

Monday 13 September 2010

Enalapril Torlan




Enalapril Torlan may be available in the countries listed below.


Ingredient matches for Enalapril Torlan



Enalapril

Enalapril maleate (a derivative of Enalapril) is reported as an ingredient of Enalapril Torlan in the following countries:


  • France

International Drug Name Search

Saturday 11 September 2010

Vital CST-222




Vital CST-222 may be available in the countries listed below.


In some countries, this medicine may only be approved for veterinary use.

Ingredient matches for Vital CST-222



Chlortetracycline

Chlortetracycline hydrochloride (a derivative of Chlortetracycline) is reported as an ingredient of Vital CST-222 in the following countries:


  • Switzerland

Sulfadimidine

Sulfadimidine is reported as an ingredient of Vital CST-222 in the following countries:


  • Switzerland

Tylosin

Tylosin phosphate (a derivative of Tylosin) is reported as an ingredient of Vital CST-222 in the following countries:


  • Switzerland

International Drug Name Search

Thursday 9 September 2010

Clemastine




In some countries, this medicine may only be approved for veterinary use.


In the US, Clemastine (clemastine systemic) is a member of the drug class antihistamines and is used to treat Allergic Reactions, Hay Fever and Urticaria.

US matches:

  • Clemastine

  • Clemastine Syrup

  • Clemastine and phenylpropanolamine

  • Clemastine y phenylpropanolamine

  • Clemastine Fumarate

Scheme

Rec.INN

ATC (Anatomical Therapeutic Chemical Classification)

D04AA14,R06AA04

CAS registry number (Chemical Abstracts Service)

0015686-51-8

Chemical Formula

C21-H26-Cl-N-O

Molecular Weight

343

Therapeutic Categories

Antiallergic agent

Histamine, H₁-receptor antagonist

Chemical Name

Pyrrolidine, 2-[2-[1-(4-chlorophenyl)-1-phenylethoxy]ethyl]-1-methyl-, [R-(R*,R*)]-

Foreign Names

  • Clemastinum (Latin)
  • Clemastin (German)
  • Clémastine (French)
  • Clemastina (Spanish)

Generic Names

  • Clemastina (OS: DCIT)
  • Clemastine (OS: BAN, USAN)
  • Clémastine (OS: DCF)
  • HS 592 (IS)
  • HS 834 (IS)
  • Mecloprodin (IS)
  • Meclopyrolin (IS)
  • Clemastine Fumarate (OS: BANM, USAN)
  • Clémastine (fumarate de) (PH: Ph. Eur. 6)
  • Clemastine Fumarate (PH: BP 2010, JP XV, USP 32, Ph. Eur. 6)
  • Clemastinfumarat (PH: Ph. Eur. 6)
  • Clemastini fumaras (PH: Ph. Eur. 6)

Brand Names

  • Clemastin
    Terapia, Romania


  • Clemastine
    Polfa Warshavskiy, Russian Federation


  • Clemastinum
    Hasco, Poland; Polfa Warszawa, Lithuania; Polfa Warszawa, Lithuania


  • Dexa Tavegil (Clemastine and Dexamethasone)
    Novartis Consumer Health, Spain


  • Tavegyl
    Novartis, Colombia; Novartis, Iceland; Novartis, Romania; Novartis Consumer Health, South Africa


  • Agasten
    Novartis, Brazil


  • Allehist-1
    Family Pharmacy, United States; Leader, United States; Medicine Shoppe, United States


  • Benanzyl
    Isei, Japan


  • Clamist
    Wander, India


  • Cle Mamallet
    Showa Yakuhin Kako, Japan


  • Clemanil
    Sandoz, Japan


  • Clemastin Actavis
    Balkanpharma, Bulgaria


  • Clemastin
    Actavis, Georgia


  • Clemastine Fumarate
    Actavis, United States; Morton Grove, United States; Novex, United States; Perrigo, United States; Sandoz, United States; Silarx, United States; Teva USA, United States


  • Clemastinum
    Aflofarm, Poland; Polfa Warszawa, Poland


  • Dayhist-1
    Drug Emporium, United States; Kroger, United States; Longs, United States; Major, United States; Perrigo, United States


  • Fuluminol
    Tatsumi Kagaku, Japan


  • Hinews
    Kyorin Rimedio, Japan


  • Inbestan
    Nichi-Iko PharmaceuticalJMA, Japan


  • Kinotomin
    Toa Eiyo, Japan


  • Magotin
    Tsuruhara Seiyaku, Japan


  • Mallermin F
    Taiyo Pharmaceutical, Japan


  • Marsthine
    Towa Yakuhin, Japan


  • Masletine
    Sioe SeiyakuShioe, Japan


  • Piloral
    Nippon Kayaku, Japan


  • Tavegil
    Dr. Fisher, Netherlands; Euro, Netherlands; Novartis, United Arab Emirates; Novartis, Bahrain; Novartis, Egypt; Novartis, Georgia; Novartis, Guyana; Novartis, Iraq; Novartis, Iran; Novartis, Jordan; Novartis, Kuwait; Novartis, Lebanon; Novartis, Oman; Novartis, Qatar; Novartis, Saudi Arabia; Novartis, Syria; Novartis, Yemen; Novartis Consumer Health, Germany; Novartis Consumer Health, Spain; Novartis Consumer Health, United Kingdom; Novartis Consumer Health, Netherlands


  • Tavegil (veterinary use)
    Novartis Animal Health, United Kingdom


  • Tavegyl
    Medis, Slovenia; Novartis, United Arab Emirates; Novartis, Bulgaria; Novartis, Bahrain; Novartis, Czech Republic; Novartis, Denmark; Novartis, Estonia; Novartis, Ghana; Novartis, Indonesia; Novartis, Iraq; Novartis, Jordan; Novartis, Japan; Novartis, Kenya; Novartis, Kuwait; Novartis, Lebanon; Novartis, Lithuania; Novartis, Latvia; Novartis, Libya; Novartis, Nigeria; Novartis, Philippines; Novartis, Portugal; Novartis, Qatar; Novartis, Russian Federation; Novartis, Saudi Arabia; Novartis, Sudan; Novartis, Sweden; Novartis, Slovakia; Novartis, Turkey; Novartis, Tanzania; Novartis, Yemen; Novartis Consumer Health, Switzerland; Novartis Consumer Health, Egypt


  • Tavist
    Novartis, India; Novartis, United States


  • Telgin G
    Takata Seiyaku, Japan


  • Xolamin
    Yoshindo, Japan

International Drug Name Search

Glossary

BANBritish Approved Name
BANMBritish Approved Name (Modified)
DCFDénomination Commune Française
DCITDenominazione Comune Italiana
ISInofficial Synonym
OSOfficial Synonym
PHPharmacopoeia Name
Rec.INNRecommended International Nonproprietary Name (World Health Organization)
USANUnited States Adopted Name

Click for further information on drug naming conventions and International Nonproprietary Names.

Drontal Plus





Dosage Form: FOR ANIMAL USE ONLY
Drontal Plus

(praziquantel/pyrantel pamoate/febantel)

Taste Tabs®

Broad Spectrum Chewable Anthelmintic Tablets for Dogs

CAUTION: Federal (U.S.A.) law restricts this drug to use by or on the order of a licensed veterinarian.



DESCRIPTION:


Drontal® Plus Taste Tabs® (praziquantel/pyrantel pamoate/febantel) Broad Spectrum Chewable Anthelmintic Tablets for Dogs are available in three tablet sizes. Each size is scored for convenient oral administration.


Each Drontal Plus Taste Tabs Tablet for Puppies and Small Dogs contains 22.7 mg praziquantel, 22.7 mg pyrantel base as pyrantel pamoate and 113.4 mg febantel.


Each Drontal Plus Taste Tabs Tablet for Medium Sized Dogs contains 68.0 mg praziquantel, 68.0 mg pyrantel base as pyrantel pamoate and 340.2 mg febantel.


Each Drontal Plus Taste Tabs Tablet for Large Dogs contains 136.0 mg praziquantel, 136.0 mg pyrantel base as pyrantel pamoate, and 680.4 mg febantel.



ACTION:


Drontal® Plus Taste Tabs® Tablets contain three active ingredients having different modes of action and spectra of activity. Praziquantel is active against cestodes (tapeworms). Praziquantel is absorbed, metabolized in the liver and excreted in the bile. Upon entering the digestive tract from the bile, cestocidal activity is exhibited.1 Following exposure to praziquantel, the tapeworm loses its ability to resist digestion by the mammalian host. Because of this, whole tapeworms, including the scolices, are very rarely passed after administration of praziquantel. In many instances only disintegrated and partially digested pieces of tapeworms will be seen in the stool. The majority of tapeworms are digested and are not found in the feces.


Pyrantel pamoate is active against hookworms and ascarids. Pyrantel pamoate acts on the cholinergic receptors of the nematode resulting in spastic paralysis. Peristaltic action of the intestinal tract then eliminates the parasite.2


Febantel is active against nematode parasites including whipworms. Febantel is rapidly absorbed and metabolized in the animal. Available information suggests that the parasite’s energy metabolism is blocked, leading to energy exchange breakdown and inhibited glucose uptake.


Laboratory efficacy and clinical studies conducted with Drontal Plus Anthelmintic Tablets demonstrate that each of the three active ingredients act independently without interference. The combined tablet formulation provides a wide spectrum of activity against the indicated species of intestinal helminths.



INDICATIONS:


Drontal® Plus (praziquantel/pyrantel pamoate/febantel) Taste Tabs® Broad Spectrum Chewable Anthelmintic Tablets are indicated for removal of Tapeworms ( Dipylidium caninum, Taenia pisiformis, Echinococcus granulosus,and removal and control of Echinococcus multilocularis) and for removal of Hookworms ( Ancylostoma caninum, Uncinaria stenocephala), Ascarids ( Toxocara canis, Toxascaris leonina), and Whipworms ( Trichuris vulpis) in dogs.



CONTRAINDICATIONS:


DO NOT USE IN PREGNANT ANIMALS. Dogs treated with elevated levels (6 consecutive days with 3 times the labeled dosage rate) of the combination of febantel and praziquantel in early pregnancy demonstrated an increased incidence of abortion and fetal abnormalities.8 The effects of Drontal® Plus Anthelmintic Tablets on pregnant animals have not been determined.


There are no known contraindications against the use of praziquantel or pyrantel pamoate in dogs.



WARNINGS:


KEEP OUT OF REACH OF CHILDREN.



PRECAUTIONS:


Strict hygienic precautions should be taken when handling dogs or feces suspected of harboring E. multilocularis. Infected dogs treated for the first time with Drontal® Plus Taste Tabs® Tablets and dogs treated at intervals greater than 28 days may shed eggs in the feces after treatment. The animal should be held in the clinic during this interval and all feces should be incinerated or autoclaved. If these procedures are not possible, the eggs can be destroyed by soaking the feces in a sodium hypochlorite (bleach) solution of 3.75% or greater.7 All areas where the animal was maintained or in contact with should be thoroughly cleaned with sodium hypochlorite and allowed to dry completely before reuse.



USE DIRECTIONS


DOSAGE: The presence of parasites should be confirmed by laboratory fecal examination. Weigh the animal before treatment. Administer the proper dosage as specified in the following table as a single oral treatment.










































DRONTAL® PLUS TASTE TABS® TABLETS DOSAGE CHARTS

*

NOT FOR USE IN PUPPIES LESS THAN 3 WEEKS OF AGE OR DOGS WEIGHING LESS THAN 2 LBS.


for Puppies and Small Dogs*


(2 - 25 lbs.)



for Medium Sized Dogs


(26 - 60 lbs.)



for Large Dogs


(45 lbs. and greater)



Body Wt. (lbs.)



No. of Tablets



Body Wt. (lbs.)



No. of Tablets



Body Wt. (lbs.)



No. of Tablets



2 – 4



0.5



26 – 30



1.0



45 – 60



1.0



5 – 7



1.0



31 – 44



1.5



61 – 90



1.5



8 – 12



1.5



45 – 60



2.0



91 – 120



2.0



13 – 18



2.0



19 – 25



2.5


    

ADMINISTRATION:


Most dogs find Drontal® Plus Taste Tabs® Tablets palatable. The tablets may be offered to the dog by hand. Alternatively tablets may be given directly by mouth or offered in a small amount of food. Fasting is neither necessary nor recommended prior to or after treatment.


RETREATMENT:


For those animals living where reinfections are likely to occur, clients should be instructed in the steps to optimize prevention; otherwise, retreatment may be necessary. This is true in cases of Dipylidium caninum where reinfection is almost certain to occur if fleas are not removed from the animal and its environment. In addition, for control of Echinococcus multilocularis, a program of regular treatment every 21 to 26 days may be indicated (see E. multilocularis section below).


ECHINOCOCCUS MULTILOCULARIS:


Echinococcus multilocularisis a tapeworm species usually found in wild canids, including foxes, coyotes and wolves. The parasite has also been identified in domestic dogs and cats and is potentially a serious public health concern because it may infect humans.


The life cycle of the parasite is based on a predator-prey relationship as depicted.



The adult tapeworm is small (1-4mm) and resides in the intestinal tract of the definitive host (wild or domestic canids). Eggs from the adult tapeworm are shed in the feces. Rodents such as mice and voles serve as the intermediate host. Eggs ingested by rodents develop in the liver, lungs and other organs to form multilocular cysts. The life cycle is completed after a canid consumes a rodent infected with cysts. Larvae within the cyst develop into adult tapeworms in the intestinal tract of the canid. Eggs may be passed in the feces of the canid approximately 28 days later.


This parasite poses a serious public health problem because of the possibility for human involvement in the life cycle. If eggs shed by an infected canid are accidentally ingested, a highly pathogenic condition (Alveolar Hydatid Disease) results from development of the cyst stage in humans.


The original geographic distribution of E. multiloculariswas primarily confined to northern areas of North America. Current evidence indicates migration of the parasite well into the continental United States.3,4


Domestic dogs living in E. multilocularisendemic areas that roam freely with the opportunity to catch wild rodents are at risk of infection. Pet owners should be advised on how to minimize this risk. Proper restraint of dogs should be encouraged, along with regular treatment with Drontal® Plus Taste Tabs® Tablets, following the dosing schedule aforementioned and precautions indicated below.


Additional information on the life cycle and epidemiology of this parasite is available in veterinary parasitology texts.5,6



DIAGNOSIS:


Diagnosis of E. multilocularis in canids is difficult. The adult tapeworm produces no clinical signs of infection. Tapeworm segments (proglottids) are usually not observed in the feces. E. multilocularis eggs, observed using microscopic fecal examination procedures, are similar in appearance to those of common species such as Taenia pisiformis. Assistance in the diagnosis of E. multilocularismay be available from a state veterinary diagnostic laboratory. Additional information regarding areas where E. multilocularisis suspected or has been confirmed may be obtained from area veterinary schools or the Centers for Disease Control in Atlanta, GA.



TREATMENT:


Dogs infected with E. multilocularis should be treated to prevent exposure of humans to infective eggs and to break the parasite’s life cycle.


The dosage of Drontal® Plus Taste Tabs® Tablets for removal of E. multilocularis is the same as that indicated for the removal of the other tapeworm species listed on the label. Laboratory efficacy studies conducted with Drontal Plus tablets have demonstrated the recommended dosage is 100% effective.


Under condition of continual exposure to wild rodents, retreatment of the dog at 21-26 day intervals is recommended to prevent the shedding of infectious eggs.



EFFICACY:


A total of 176 dogs and puppies with naturally acquired or experimental parasite infections were included in 4 well-controlled laboratory studies to establish the efficacy of Drontal® Plus Anthelmintic Tablets. In addition, 103 dogs and puppies were included in clinical field studies conducted in 5 veterinary clinics at different geographic locations throughout the United States to further evaluate safety and efficacy. These studies included dogs of various sizes, ages and breeds. Data from these studies demonstrated Drontal Plus Anthelmintic Tablets are safe and efficacious for the removal of the parasite species indicated on the label when used as directed. Results obtained in the laboratory and clinical studies indicate small numbers of hookworm or roundworm eggs may be passed in the feces for up to 7 days after treatment although the worms themselves were eliminated. A follow-up fecal examination should be conducted 2 to 4 weeks after treatment to determine the need for retreatment.


Palatability:


Palatability studies with Drontal® Plus Taste Tabs® Tablets were conducted at 3 different veterinary clinics in the United States. These studies included a total of 151 dogs (65 males / 86 females) representing 34 different breeds with body weights ranging from 3.8 – 190 lbs. The tablets were offered free-choice to the dogs by their owners and over 89% of the dogs willingly consumed the tablets.



ADVERSE REACTIONS:


None of the 103 dogs treated with Drontal® Plus Anthelmintic Tablets in the clinical field studies exhibited drug-related side effects. Of the 40 dogs treated with Drontal Plus Taste Tabs® Tablets in laboratory studies, two dogs exhibited vomiting, one puppy exhibited bloody/mucoid stool and one puppy exhibited watery/profuse stool.


For customer service or to obtain product information, including Material Safety Data Sheet, call 1-800-633-3796. For medical emergencies or to report adverse reactions, call 1-800-422-9874.



ANIMAL SAFETY:


Controlled safety evaluations have been conducted in dogs with Drontal® Plus (praziquantel/pyrantel pamoate/febantel) Anthelmintic Tablets. Dogs receiving up to 5 times the label dosage (35 mg praziquantel, 35 mg pyrantel pamoate and 179 mg febantel per kg of body weight) for 3 consecutive days (3 times the label duration) showed clinical signs of vomition and non-formed stools. One dog receiving a 3 times labeled dose had elevated SGPT, SGOT, CPK and GGT readings (outside of normal range) at 6 days post-treatment. No additional findings were noted in hematology/clinical chemistry parameters nor were there any treatment-related histological lesions. Vomition was the only side effect observed when dogs received a single treatment of 61 mg praziquantel, 61 mg pyrantel pamoate and 305 mg febantel/kg with one dog having an elevated SGPT reading (outside of normal range) at 24 hours post-treatment which had returned to normal by 7 days.



STORAGE CONDITIONS:


Drontal® Plus Taste Tabs® Tablets should be stored at or below 77 °F (25 °C).


Un-blistered whole or partial tablets should be stored in a tightly sealed container.



How is Drontal Plus Supplied


Drontal® Plus Taste Tabs® Tablets are available in three tablet sizes:


Code    08758428: 40 tabs/box for Puppies and Small Dogs


Code    08892051: 40 tabs/box for Medium Sized Dogs


Code    08892078: 30 tabs /box for Large Dogs



REFERENCES:


1 Andrews P. 1976. Pharmacokinetic Studies with DRONCIT® in Animals Using a Biological Assay. Veterinary Medical Review. 2:154-165.


2 Campbell WC. 1986. The Chemotherapy of Parasitic Infections. J. Parasit. 72(1):45-61.


3 Hildreth MB Johnson MD and Kazacos KR. 1991. A Zoonosis of Increasing Concern in the United States. Compendium for Cont. Ed. 13(5): 727-740.


4 PD Carney WP and Woods CE. 1970. Studies on Sylvatic Echinococcosis, Ill. Host Occurrence and Geographic Distribution of Echinococcus multilocularisin the North Central United States. J. Parasit. 56(6): 1141-1150.


5 Georgi JR and Georgi ME. 1990. Parasitology for Veterinarians. W.B. Saunders Co. 118-138.


6 Soulsby EJL. 1982. Helminths, Arthropods and Protozoa of Domesticated Animals. 7th Edition. Lea & Febiger. 118-138.


7 Craig PS and McPharson CNL. 1988. Sodium Hypochlorite as an Ovicide for Echinococcus. Ann Trop Med. and Parasit. 82(2): 211-213.


8 Freedom of Information Summary (FOI) NADA 133-953 Vercom Paste (febantel and praziquantel).


 



Bayer HealthCare LLC


Animal Health Division


Shawnee Mission, Kansas 66201 USA


NADA 141-007, Approved by FDA


January, 2006 ©2006 Bayer HealthCare LLC


R.0 Bayer, the Bayer Cross, Drontal, and Taste


12894 Tabs are registered trademarks of Bayer



Principal Display Panels




Principal Display Panels




Principal Display Panels




Principal Display Panel




Principal Display Panel










Drontal Plus TASTE TABS 
praziquantel/pyrantel pamoate/febantel  tablet, chewable










Product Information
Product TypePRESCRIPTION ANIMAL DRUGNDC Product Code (Source)0859-2168
Route of AdministrationORALDEA Schedule    














Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
PRAZIQUANTEL (PRAZIQUANTEL)PRAZIQUANTEL22.7 mg
PYRANTEL PAMOATE (PYRANTEL)PYRANTEL PAMOATE22.7 mg
FEBANTEL (FEBANTEL)FEBANTEL113.4 mg





Inactive Ingredients
Ingredient NameStrength
No Inactive Ingredients Found


















Product Characteristics
ColorBROWNScore2 pieces
ShapeFREEFORM (Bone)Size20mm
FlavorMEAT (Artificial Beef)Imprint CodeD10
Contains      














Packaging
#NDCPackage DescriptionMultilevel Packaging
10859-2168-014 BLISTER PACK In 1 BOXcontains a BLISTER PACK
110 TABLET In 1 BLISTER PACKThis package is contained within the BOX (0859-2168-01)










Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
NADANADA14100701/12/200612/28/2010







Drontal Plus TASTE TABS 
praziquantel/pyrantel pamoate/febantel  tablet, chewable










Product Information
Product TypePRESCRIPTION ANIMAL DRUGNDC Product Code (Source)0859-2169
Route of AdministrationORALDEA Schedule    














Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
PRAZIQUANTEL (PRAZIQUANTEL)PRAZIQUANTEL68 mg
PYRANTEL PAMOATE (PYRANTEL)PYRANTEL PAMOATE68 mg
FEBANTEL (FEBANTEL)FEBANTEL340.2 mg





Inactive Ingredients
Ingredient NameStrength
No Inactive Ingredients Found


















Product Characteristics
ColorBROWNScore2 pieces
ShapeFREEFORM (Bone)Size25mm
FlavorMEAT (Artificial Beef)Imprint CodeDP30
Contains      














Packaging
#NDCPackage DescriptionMultilevel Packaging
10859-2169-014 BLISTER PACK In 1 BOXcontains a BLISTER PACK
110 TABLET In 1 BLISTER PACKThis package is contained within the BOX (0859-2169-01)










Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
NADANADA14100701/12/200612/28/2010







Drontal Plus TASTE TABS 
praziquantel/pyrantel pamoate/febantel  tablet, chewable










Product Information
Product TypePRESCRIPTION ANIMAL DRUGNDC Product Code (Source)0859-2182
Route of AdministrationORALDEA Schedule    














Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
PRAZIQUANTEL (PRAZIQUANTEL)PRAZIQUANTEL136 mg
PYRANTEL PAMOATE (PYRANTEL)PYRANTEL PAMOATE136 mg
FEBANTEL (FEBANTEL)FEBANTEL680.4 mg





Inactive Ingredients
Ingredient NameStrength
No Inactive Ingredients Found


















Product Characteristics
ColorBROWNScore2 pieces
ShapeFREEFORM (Bone)Size32mm
FlavorMEAT (Artificial Beef)Imprint CodeDP60
Contains      














Packaging
#NDCPackage DescriptionMultilevel Packaging
10859-2182-013 BLISTER PACK In 1 BOXcontains a BLISTER PACK
110 TABLET In 1 BLISTER PACKThis package is contained within the BOX (0859-2182-01)










Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
NADANADA14100701/12/2006







Drontal Plus TASTE TABS 
praziquantel/pyrantel pamoate/febantel  tablet, chewable










Product Information
Product TypePRESCRIPTION ANIMAL DRUGNDC Product Code (Source)0859-2180
Route of AdministrationORALDEA Schedule    














Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
PRAZIQUANTEL (PRAZIQUANTEL)PRAZIQUANTEL22.7 mg
PYRANTEL PAMOATE (PYRANTEL)PYRANTEL PAMOATE22.7 mg
FEBANTEL (FEBANTEL)FEBANTEL113.4 mg





Inactive Ingredients
Ingredient NameStrength
No Inactive Ingredients Found


















Product Characteristics
ColorBROWNScore2 pieces
ShapeFREEFORM (Bone)Size20mm
FlavorMEAT (Artificial Beef)Imprint CodeD10
Contains      














Packaging
#NDCPackage DescriptionMultilevel Packaging
10859-2180-014 BLISTER PACK In 1 BOXcontains a BLISTER PACK
110 TABLET In 1 BLISTER PACKThis package is contained within the BOX (0859-2180-01)










Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
NADANADA14100701/12/2006







Drontal Plus TASTE TABS 
praziquantel/pyrantel pamoate/febantel  tablet, chewable










Product Information
Product TypePRESCRIPTION ANIMAL DRUGNDC Product Code (Source)0859-2181
Route of AdministrationORALDEA Schedule    














Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
PRAZIQUANTEL (PRAZIQUANTEL)PRAZIQUANTEL68 mg
PYRANTEL PAMOATE (PYRANTEL)PYRANTEL PAMOATE68 mg
FEBANTEL (FEBANTEL)FEBANTEL340.2 mg





Inactive Ingredients
Ingredient NameStrength
No Inactive Ingredients Found


















Product Characteristics
ColorBROWNScore2 pieces
ShapeFREEFORM (Bone)Size25mm
FlavorMEAT (Artificial Beef)Imprint CodeDP30
Contains      














Packaging
#NDCPackage DescriptionMultilevel Packaging
10859-2181-014 BLISTER PACK In 1 BOXcontains a BLISTER PACK
110 TABLET In 1 BLISTER PACKThis package is contained within the BOX (0859-2181-01)










Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
NADANADA14100701/12/200612/28/2010


Labeler - Bayer HealthCare LLC Animal Health Division (152266193)
Revised: 05/2009Bayer HealthCare LLC Animal Health Division



Ciprofloxacina Tetrafarma




Ciprofloxacina Tetrafarma may be available in the countries listed below.


Ingredient matches for Ciprofloxacina Tetrafarma



Ciprofloxacin

Ciprofloxacin is reported as an ingredient of Ciprofloxacina Tetrafarma in the following countries:


  • Portugal

International Drug Name Search

Wednesday 8 September 2010

Lansoprazolo ratiopharm




Lansoprazolo ratiopharm may be available in the countries listed below.


Ingredient matches for Lansoprazolo ratiopharm



Lansoprazole

Lansoprazole is reported as an ingredient of Lansoprazolo ratiopharm in the following countries:


  • Italy

International Drug Name Search

Tuesday 7 September 2010

DG-6




DG-6 may be available in the countries listed below.


Ingredient matches for DG-6



Lapirium Chloride

Lapirium Chloride is reported as an ingredient of DG-6 in the following countries:


  • Argentina

International Drug Name Search

Sunday 5 September 2010

Zomig Rapimelt




Zomig Rapimelt may be available in the countries listed below.


UK matches:

  • Zomig Rapimelt 2.5mg
  • Zomig Rapimelt 5mg Orodispersible Tablets
  • Zomig Rapimelt 2.5mg (SPC)
  • Zomig Rapimelt 5 mg Orodispersible Tablets (SPC)

Ingredient matches for Zomig Rapimelt



Zolmitriptan

Zolmitriptan is reported as an ingredient of Zomig Rapimelt in the following countries:


  • Austria

  • Czech Republic

  • Hong Kong

  • Iceland

  • Israel

  • Italy

  • Portugal

  • Slovenia

  • Sweden

  • United Kingdom

International Drug Name Search

Glossary

SPC Summary of Product Characteristics (UK)

Click for further information on drug naming conventions and International Nonproprietary Names.

Canthacur Liq 0.7%




Canthacur Liq 0.7% may be available in the countries listed below.


Ingredient matches for Canthacur Liq 0.7%



Cantharidin

Cantharidin is reported as an ingredient of Canthacur Liq 0.7% in the following countries:


  • Canada

International Drug Name Search

Thursday 2 September 2010

Dilacoran




Dilacoran may be available in the countries listed below.


Ingredient matches for Dilacoran



Verapamil

Verapamil hydrochloride (a derivative of Verapamil) is reported as an ingredient of Dilacoran in the following countries:


  • Mexico

International Drug Name Search