JP2000503306A - 駆虫ペースト - Google Patents
駆虫ペーストInfo
- Publication number
- JP2000503306A JP2000503306A JP9525637A JP52563797A JP2000503306A JP 2000503306 A JP2000503306 A JP 2000503306A JP 9525637 A JP9525637 A JP 9525637A JP 52563797 A JP52563797 A JP 52563797A JP 2000503306 A JP2000503306 A JP 2000503306A
- Authority
- JP
- Japan
- Prior art keywords
- spp
- paste
- anthelmintic
- glycerin
- horses
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
- 230000000507 anthelmentic effect Effects 0.000 title claims abstract description 9
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 claims abstract description 14
- 150000001875 compounds Chemical class 0.000 claims abstract description 9
- 235000011187 glycerol Nutrition 0.000 claims abstract description 7
- 229920002261 Corn starch Polymers 0.000 claims abstract description 6
- 241000283086 Equidae Species 0.000 claims abstract description 6
- 239000008120 corn starch Substances 0.000 claims abstract description 6
- 241000282472 Canis lupus familiaris Species 0.000 claims abstract description 5
- 241000282326 Felis catus Species 0.000 claims abstract description 5
- 229920002472 Starch Polymers 0.000 claims 1
- 229940124339 anthelmintic agent Drugs 0.000 claims 1
- 239000000921 anthelmintic agent Substances 0.000 claims 1
- 235000019698 starch Nutrition 0.000 claims 1
- 239000008107 starch Substances 0.000 claims 1
- 150000004885 piperazines Chemical class 0.000 abstract 1
- 239000000203 mixture Substances 0.000 description 9
- 238000009472 formulation Methods 0.000 description 5
- FSVJFNAIGNNGKK-UHFFFAOYSA-N 2-[cyclohexyl(oxo)methyl]-3,6,7,11b-tetrahydro-1H-pyrazino[2,1-a]isoquinolin-4-one Chemical compound C1C(C2=CC=CC=C2CC2)N2C(=O)CN1C(=O)C1CCCCC1 FSVJFNAIGNNGKK-UHFFFAOYSA-N 0.000 description 4
- QRJZGVVKGFIGLI-UHFFFAOYSA-N 2-phenylguanidine Chemical class NC(=N)NC1=CC=CC=C1 QRJZGVVKGFIGLI-UHFFFAOYSA-N 0.000 description 4
- 125000003545 alkoxy group Chemical group 0.000 description 4
- 150000001556 benzimidazoles Chemical class 0.000 description 4
- 229910052739 hydrogen Inorganic materials 0.000 description 4
- 239000001257 hydrogen Substances 0.000 description 4
- 229960002957 praziquantel Drugs 0.000 description 4
- 150000005326 tetrahydropyrimidines Chemical class 0.000 description 4
- 125000003118 aryl group Chemical group 0.000 description 3
- 125000000753 cycloalkyl group Chemical group 0.000 description 3
- 150000002431 hydrogen Chemical class 0.000 description 3
- -1 phenylthio, phenylsulfinyl Chemical group 0.000 description 3
- 125000000547 substituted alkyl group Chemical group 0.000 description 3
- 241000244186 Ascaris Species 0.000 description 2
- RAOCRURYZCVHMG-UHFFFAOYSA-N N-(6-propoxy-1H-benzimidazol-2-yl)carbamic acid methyl ester Chemical compound CCCOC1=CC=C2N=C(NC(=O)OC)NC2=C1 RAOCRURYZCVHMG-UHFFFAOYSA-N 0.000 description 2
- 241000244206 Nematoda Species 0.000 description 2
- GLUUGHFHXGJENI-UHFFFAOYSA-N Piperazine Chemical compound C1CNCCN1 GLUUGHFHXGJENI-UHFFFAOYSA-N 0.000 description 2
- 235000005775 Setaria Nutrition 0.000 description 2
- 241000232088 Setaria <nematode> Species 0.000 description 2
- 241001617580 Stephanurus Species 0.000 description 2
- ZVIDWFUBDDXAJA-UHFFFAOYSA-N [2-(methoxycarbonylamino)-3h-benzimidazol-5-yl] 4-fluorobenzenesulfonate Chemical compound C1=C2NC(NC(=O)OC)=NC2=CC=C1OS(=O)(=O)C1=CC=C(F)C=C1 ZVIDWFUBDDXAJA-UHFFFAOYSA-N 0.000 description 2
- 229960002669 albendazole Drugs 0.000 description 2
- HXHWSAZORRCQMX-UHFFFAOYSA-N albendazole Chemical compound CCCSC1=CC=C2NC(NC(=O)OC)=NC2=C1 HXHWSAZORRCQMX-UHFFFAOYSA-N 0.000 description 2
- 125000003342 alkenyl group Chemical group 0.000 description 2
- 125000004414 alkyl thio group Chemical group 0.000 description 2
- 125000000304 alkynyl group Chemical group 0.000 description 2
- 244000079386 endoparasite Species 0.000 description 2
- HDDSHPAODJUKPD-UHFFFAOYSA-N fenbendazole Chemical compound C1=C2NC(NC(=O)OC)=NC2=CC=C1SC1=CC=CC=C1 HDDSHPAODJUKPD-UHFFFAOYSA-N 0.000 description 2
- 229960005473 fenbendazole Drugs 0.000 description 2
- 239000004615 ingredient Substances 0.000 description 2
- 229950001484 luxabendazole Drugs 0.000 description 2
- BEZZFPOZAYTVHN-UHFFFAOYSA-N oxfendazole Chemical compound C=1C=C2NC(NC(=O)OC)=NC2=CC=1S(=O)C1=CC=CC=C1 BEZZFPOZAYTVHN-UHFFFAOYSA-N 0.000 description 2
- 229960004454 oxfendazole Drugs 0.000 description 2
- 230000001717 pathogenic effect Effects 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- 239000003755 preservative agent Substances 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- NVEPPWDVLBMNMB-SNAWJCMRSA-N 1-methyl-2-[(e)-2-(3-methylthiophen-2-yl)ethenyl]-5,6-dihydro-4h-pyrimidine Chemical compound CN1CCCN=C1\C=C\C1=C(C)C=CS1 NVEPPWDVLBMNMB-SNAWJCMRSA-N 0.000 description 1
- WCBVUETZRWGIJQ-UHFFFAOYSA-N 2-[[(methoxycarbonylamino)-(2-nitro-5-propylsulfanylanilino)methylidene]amino]ethanesulfonic acid Chemical compound CCCSC1=CC=C([N+]([O-])=O)C(NC(NC(=O)OC)=NCCS(O)(=O)=O)=C1 WCBVUETZRWGIJQ-UHFFFAOYSA-N 0.000 description 1
- 241001465677 Ancylostomatoidea Species 0.000 description 1
- 241000204727 Ascaridia Species 0.000 description 1
- 241000244203 Caenorhabditis elegans Species 0.000 description 1
- 241000253350 Capillaria Species 0.000 description 1
- 241000242722 Cestoda Species 0.000 description 1
- 241001278326 Craterostomum Species 0.000 description 1
- 241000244152 Cyclophyllidea Species 0.000 description 1
- 241001389925 Digenea <Rhodophyta> Species 0.000 description 1
- 241001222688 Diorchis Species 0.000 description 1
- 241001137876 Diphyllobothrium Species 0.000 description 1
- 241000243990 Dirofilaria Species 0.000 description 1
- 235000003550 Dracunculus Nutrition 0.000 description 1
- 241000316827 Dracunculus <angiosperm> Species 0.000 description 1
- 241000244160 Echinococcus Species 0.000 description 1
- 241000498256 Enterobius Species 0.000 description 1
- 241001263042 Fasciola sp. Species 0.000 description 1
- HMCCXLBXIJMERM-UHFFFAOYSA-N Febantel Chemical compound C1=C(NC(NC(=O)OC)=NC(=O)OC)C(NC(=O)COC)=CC(SC=2C=CC=CC=2)=C1 HMCCXLBXIJMERM-UHFFFAOYSA-N 0.000 description 1
- 241000986243 Filaroides Species 0.000 description 1
- 241000315566 Habronema Species 0.000 description 1
- 241001464082 Hydatigera Species 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- 241000520690 Mesocestoides Species 0.000 description 1
- 241000274183 Micromeria Species 0.000 description 1
- 241000986227 Muellerius Species 0.000 description 1
- YRWLZFXJFBZBEY-UHFFFAOYSA-N N-(6-butyl-1H-benzimidazol-2-yl)carbamic acid methyl ester Chemical compound CCCCC1=CC=C2N=C(NC(=O)OC)NC2=C1 YRWLZFXJFBZBEY-UHFFFAOYSA-N 0.000 description 1
- 241000520254 Oesophagodontus Species 0.000 description 1
- 241000243981 Onchocerca Species 0.000 description 1
- 241000242716 Opisthorchis Species 0.000 description 1
- 241001221709 Oxyurida Species 0.000 description 1
- 241000904715 Oxyuris Species 0.000 description 1
- 241000545637 Parafilaroides Species 0.000 description 1
- 241000244187 Parascaris Species 0.000 description 1
- 241001617421 Protostrongylus Species 0.000 description 1
- 241001137874 Pseudophyllidea Species 0.000 description 1
- 241001222586 Schistocephalus Species 0.000 description 1
- 241000242678 Schistosoma Species 0.000 description 1
- 241000203992 Spirometra Species 0.000 description 1
- 241000244042 Spirurida Species 0.000 description 1
- 241001126263 Strongylidae Species 0.000 description 1
- 241000244174 Strongyloides Species 0.000 description 1
- 241001477954 Thelazia Species 0.000 description 1
- 241000607216 Toxascaris Species 0.000 description 1
- 241000244031 Toxocara Species 0.000 description 1
- 241000869417 Trematodes Species 0.000 description 1
- 241000243774 Trichinella Species 0.000 description 1
- 241001489151 Trichuris Species 0.000 description 1
- 241000530048 Triodontophorus Species 0.000 description 1
- 241000571986 Uncinaria Species 0.000 description 1
- 241000607479 Yersinia pestis Species 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- 238000003975 animal breeding Methods 0.000 description 1
- 244000052616 bacterial pathogen Species 0.000 description 1
- 125000003236 benzoyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C(*)=O 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 238000009395 breeding Methods 0.000 description 1
- 230000001488 breeding effect Effects 0.000 description 1
- LGUDKOQUWIHXOV-UHFFFAOYSA-N epsiprantel Chemical compound C1C(C2=CC=CC=C2CCC2)N2C(=O)CN1C(=O)C1CCCCC1 LGUDKOQUWIHXOV-UHFFFAOYSA-N 0.000 description 1
- 229960005362 epsiprantel Drugs 0.000 description 1
- 230000002349 favourable effect Effects 0.000 description 1
- 229960005282 febantel Drugs 0.000 description 1
- 125000001188 haloalkyl group Chemical group 0.000 description 1
- 229910052736 halogen Inorganic materials 0.000 description 1
- 150000002367 halogens Chemical class 0.000 description 1
- 244000144972 livestock Species 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 229960003439 mebendazole Drugs 0.000 description 1
- OPXLLQIJSORQAM-UHFFFAOYSA-N mebendazole Chemical compound C=1C=C2NC(NC(=O)OC)=NC2=CC=1C(=O)C1=CC=CC=C1 OPXLLQIJSORQAM-UHFFFAOYSA-N 0.000 description 1
- 230000029052 metamorphosis Effects 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 229960005121 morantel Drugs 0.000 description 1
- 229960000535 oxantel Drugs 0.000 description 1
- VRYKTHBAWRESFI-VOTSOKGWSA-N oxantel Chemical compound CN1CCCN=C1\C=C\C1=CC=CC(O)=C1 VRYKTHBAWRESFI-VOTSOKGWSA-N 0.000 description 1
- 229960002762 oxibendazole Drugs 0.000 description 1
- 229950007337 parbendazole Drugs 0.000 description 1
- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- 125000003170 phenylsulfonyl group Chemical group C1(=CC=CC=C1)S(=O)(=O)* 0.000 description 1
- IWELDVXSEVIIGI-UHFFFAOYSA-N piperazin-2-one Chemical class O=C1CNCCN1 IWELDVXSEVIIGI-UHFFFAOYSA-N 0.000 description 1
- 230000002265 prevention Effects 0.000 description 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
- 229960005134 pyrantel Drugs 0.000 description 1
- YSAUAVHXTIETRK-AATRIKPKSA-N pyrantel Chemical compound CN1CCCN=C1\C=C\C1=CC=CS1 YSAUAVHXTIETRK-AATRIKPKSA-N 0.000 description 1
- 241000894007 species Species 0.000 description 1
- 125000001544 thienyl group Chemical group 0.000 description 1
- 230000001988 toxicity Effects 0.000 description 1
- 231100000419 toxicity Toxicity 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/498—Pyrazines or piperazines ortho- and peri-condensed with carbocyclic ring systems, e.g. quinoxaline, phenazine
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/0012—Galenical forms characterised by the site of application
- A61K9/0053—Mouth and digestive tract, i.e. intraoral and peroral administration
- A61K9/0056—Mouth soluble or dispersible forms; Suckable, eatable, chewable coherent forms; Forms rapidly disintegrating in the mouth; Lozenges; Lollipops; Bite capsules; Baked products; Baits or other oral forms for animals
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P33/00—Antiparasitic agents
- A61P33/10—Anthelmintics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K47/00—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
- A61K47/06—Organic compounds, e.g. natural or synthetic hydrocarbons, polyolefins, mineral oil, petrolatum or ozokerite
- A61K47/08—Organic compounds, e.g. natural or synthetic hydrocarbons, polyolefins, mineral oil, petrolatum or ozokerite containing oxygen, e.g. ethers, acetals, ketones, quinones, aldehydes, peroxides
- A61K47/10—Alcohols; Phenols; Salts thereof, e.g. glycerol; Polyethylene glycols [PEG]; Poloxamers; PEG/POE alkyl ethers
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K47/00—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
- A61K47/30—Macromolecular organic or inorganic compounds, e.g. inorganic polyphosphates
- A61K47/36—Polysaccharides; Derivatives thereof, e.g. gums, starch, alginate, dextrin, hyaluronic acid, chitosan, inulin, agar or pectin
Landscapes
- Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Life Sciences & Earth Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Epidemiology (AREA)
- Physiology (AREA)
- Nutrition Science (AREA)
- Zoology (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Tropical Medicine & Parasitology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Medicinal Preparation (AREA)
- Processing Of Solid Wastes (AREA)
- Fertilizers (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
Abstract
Description
Claims (1)
- 【特許請求の範囲】 1.馬、犬及びネコ用の、ヘキサヒドロピラジノ−誘導体をベースとする駆虫 ペーストにおいて、該活性化合物のほかに、ペースト形成用の補助剤としてコー ンスターチ及びグリセリンを含むことを特徴とする前記駆虫ペースト。 2.駆虫ペーストが、5乃至30%の重量濃度で活性化合物、10乃至30% の重量濃度でコーンスターチ及び40乃至80%の重量濃度でグリセリンを含ん でなることを特徴とする、請求の範囲1に記載の馬、犬及びネコ用の駆虫ペース ト。
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE19601263.5 | 1996-01-16 | ||
DE19601263A DE19601263A1 (de) | 1996-01-16 | 1996-01-16 | Anthelmintische Paste |
PCT/EP1997/000006 WO1997025976A1 (de) | 1996-01-16 | 1997-01-03 | Anthelminthische paste |
Publications (3)
Publication Number | Publication Date |
---|---|
JP2000503306A true JP2000503306A (ja) | 2000-03-21 |
JP2000503306A5 JP2000503306A5 (ja) | 2004-10-28 |
JP4143121B2 JP4143121B2 (ja) | 2008-09-03 |
Family
ID=7782814
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP52563797A Expired - Fee Related JP4143121B2 (ja) | 1996-01-16 | 1997-01-03 | 駆虫ペースト |
Country Status (15)
Country | Link |
---|---|
US (1) | US6025357A (ja) |
EP (1) | EP0877598B1 (ja) |
JP (1) | JP4143121B2 (ja) |
KR (1) | KR100451857B1 (ja) |
AT (1) | ATE201979T1 (ja) |
AU (1) | AU703567B2 (ja) |
BR (1) | BR9706976A (ja) |
CA (1) | CA2242972C (ja) |
DE (2) | DE19601263A1 (ja) |
DK (1) | DK0877598T3 (ja) |
ES (1) | ES2157551T3 (ja) |
HU (1) | HU227817B1 (ja) |
NZ (1) | NZ325850A (ja) |
PT (1) | PT877598E (ja) |
WO (1) | WO1997025976A1 (ja) |
Families Citing this family (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6207179B1 (en) * | 2000-05-18 | 2001-03-27 | Phoenix Scientific, Inc. | Parasiticidal formulation for animals and a method of making this formulation |
DE10358525A1 (de) | 2003-12-13 | 2005-07-07 | Bayer Healthcare Ag | Endoparasitizide Mittel zur topischen Applikation |
DE102005011779A1 (de) * | 2005-03-11 | 2006-09-14 | Bayer Healthcare Ag | Endoparasitizide Mittel |
Family Cites Families (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4117156A (en) * | 1975-07-18 | 1978-09-26 | Ciba-Geigy Ag | Anthelmintic preparations |
US4447414A (en) * | 1982-12-21 | 1984-05-08 | Cutter Laboratories, Inc. | Carnivore anthelmintics |
US4675174A (en) * | 1985-08-16 | 1987-06-23 | Alza Corporation | Veterinary dispenser delivering beneficial agent by gas power generated in situ |
DE3705227A1 (de) * | 1987-02-19 | 1988-09-01 | Bayer Ag | Anthelminthische wirkstoffkombinationen |
HU217811B (hu) * | 1991-12-23 | 2000-04-28 | András Selmeczi | Eljárás metil-5(6)-benzoil-2-benzimidazol-karbamátot tartalmazó gélformájú, antiparazitikus hatású állatgyógyászati készítmény előállítására |
AUPM969994A0 (en) * | 1994-11-28 | 1994-12-22 | Virbac S.A. | Equine anthelmintic formulations |
-
1996
- 1996-01-16 DE DE19601263A patent/DE19601263A1/de not_active Withdrawn
-
1997
- 1997-01-03 US US09/101,931 patent/US6025357A/en not_active Expired - Lifetime
- 1997-01-03 ES ES97900555T patent/ES2157551T3/es not_active Expired - Lifetime
- 1997-01-03 BR BR9706976-0A patent/BR9706976A/pt not_active IP Right Cessation
- 1997-01-03 NZ NZ325850A patent/NZ325850A/xx not_active IP Right Cessation
- 1997-01-03 PT PT97900555T patent/PT877598E/pt unknown
- 1997-01-03 AU AU13093/97A patent/AU703567B2/en not_active Ceased
- 1997-01-03 AT AT97900555T patent/ATE201979T1/de active
- 1997-01-03 CA CA002242972A patent/CA2242972C/en not_active Expired - Fee Related
- 1997-01-03 HU HU9901023A patent/HU227817B1/hu not_active IP Right Cessation
- 1997-01-03 DE DE59703789T patent/DE59703789D1/de not_active Expired - Lifetime
- 1997-01-03 WO PCT/EP1997/000006 patent/WO1997025976A1/de active IP Right Grant
- 1997-01-03 EP EP97900555A patent/EP0877598B1/de not_active Expired - Lifetime
- 1997-01-03 KR KR10-1998-0704695A patent/KR100451857B1/ko not_active IP Right Cessation
- 1997-01-03 JP JP52563797A patent/JP4143121B2/ja not_active Expired - Fee Related
- 1997-01-03 DK DK97900555T patent/DK0877598T3/da active
Also Published As
Publication number | Publication date |
---|---|
HU227817B1 (en) | 2012-03-28 |
ES2157551T3 (es) | 2001-08-16 |
DE59703789D1 (en) | 2001-07-19 |
ATE201979T1 (de) | 2001-06-15 |
EP0877598A1 (de) | 1998-11-18 |
JP4143121B2 (ja) | 2008-09-03 |
BR9706976A (pt) | 2000-01-04 |
US6025357A (en) | 2000-02-15 |
DE19601263A1 (de) | 1997-07-17 |
CA2242972C (en) | 2005-03-15 |
EP0877598B1 (de) | 2001-06-13 |
HUP9901023A2 (hu) | 1999-07-28 |
KR100451857B1 (ko) | 2005-07-07 |
NZ325850A (en) | 1999-02-25 |
CA2242972A1 (en) | 1997-07-24 |
DK0877598T3 (da) | 2001-07-23 |
HUP9901023A3 (en) | 1999-11-29 |
PT877598E (pt) | 2001-11-30 |
AU703567B2 (en) | 1999-03-25 |
AU1309397A (en) | 1997-08-11 |
KR19990076602A (ko) | 1999-10-15 |
WO1997025976A1 (de) | 1997-07-24 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
US7763583B2 (en) | Endoparasiticidal compositions for topical application | |
CN102215824B (zh) | 具有延迟释放的固体药物制剂 | |
BRPI0111914B1 (pt) | artigos moldados extrudados à base de amido para absorção oral voluntária pelos animais e processo para preparação dos mesmos | |
JP5232635B2 (ja) | 内部寄生虫駆除剤 | |
EP0279343B1 (de) | Anthelminthische Wirkstoffkombinationen | |
JP2012107024A (ja) | 殺内部寄生虫剤 | |
JP2000503306A (ja) | 駆虫ペースト | |
JP2000515519A (ja) | ヘキサヒドロピラジン誘導体の経口投与できる顆粒剤 | |
WO1992016210A1 (fr) | Nouvelles compositions liquides a base de derives de la piperidine substitues en 1,4 | |
KR100569858B1 (ko) | 경피투여용 항구토제 조성물 |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
A131 | Notification of reasons for refusal |
Free format text: JAPANESE INTERMEDIATE CODE: A131 Effective date: 20070724 |
|
A521 | Request for written amendment filed |
Free format text: JAPANESE INTERMEDIATE CODE: A523 Effective date: 20071024 |
|
RD02 | Notification of acceptance of power of attorney |
Free format text: JAPANESE INTERMEDIATE CODE: A7422 Effective date: 20080327 |
|
TRDD | Decision of grant or rejection written | ||
A01 | Written decision to grant a patent or to grant a registration (utility model) |
Free format text: JAPANESE INTERMEDIATE CODE: A01 Effective date: 20080610 |
|
A01 | Written decision to grant a patent or to grant a registration (utility model) |
Free format text: JAPANESE INTERMEDIATE CODE: A01 |
|
A61 | First payment of annual fees (during grant procedure) |
Free format text: JAPANESE INTERMEDIATE CODE: A61 Effective date: 20080616 |
|
FPAY | Renewal fee payment (event date is renewal date of database) |
Free format text: PAYMENT UNTIL: 20110620 Year of fee payment: 3 |
|
R150 | Certificate of patent or registration of utility model |
Free format text: JAPANESE INTERMEDIATE CODE: R150 |
|
S111 | Request for change of ownership or part of ownership |
Free format text: JAPANESE INTERMEDIATE CODE: R313113 |
|
FPAY | Renewal fee payment (event date is renewal date of database) |
Free format text: PAYMENT UNTIL: 20110620 Year of fee payment: 3 |
|
R360 | Written notification for declining of transfer of rights |
Free format text: JAPANESE INTERMEDIATE CODE: R360 |
|
FPAY | Renewal fee payment (event date is renewal date of database) |
Free format text: PAYMENT UNTIL: 20110620 Year of fee payment: 3 |
|
R360 | Written notification for declining of transfer of rights |
Free format text: JAPANESE INTERMEDIATE CODE: R360 |
|
R371 | Transfer withdrawn |
Free format text: JAPANESE INTERMEDIATE CODE: R371 |
|
S111 | Request for change of ownership or part of ownership |
Free format text: JAPANESE INTERMEDIATE CODE: R313113 |
|
FPAY | Renewal fee payment (event date is renewal date of database) |
Free format text: PAYMENT UNTIL: 20110620 Year of fee payment: 3 |
|
R350 | Written notification of registration of transfer |
Free format text: JAPANESE INTERMEDIATE CODE: R350 |
|
FPAY | Renewal fee payment (event date is renewal date of database) |
Free format text: PAYMENT UNTIL: 20110620 Year of fee payment: 3 |
|
FPAY | Renewal fee payment (event date is renewal date of database) |
Free format text: PAYMENT UNTIL: 20110620 Year of fee payment: 3 |
|
FPAY | Renewal fee payment (event date is renewal date of database) |
Free format text: PAYMENT UNTIL: 20120620 Year of fee payment: 4 |
|
FPAY | Renewal fee payment (event date is renewal date of database) |
Free format text: PAYMENT UNTIL: 20120620 Year of fee payment: 4 |
|
FPAY | Renewal fee payment (event date is renewal date of database) |
Free format text: PAYMENT UNTIL: 20130620 Year of fee payment: 5 |
|
FPAY | Renewal fee payment (event date is renewal date of database) |
Free format text: PAYMENT UNTIL: 20130620 Year of fee payment: 5 |
|
S111 | Request for change of ownership or part of ownership |
Free format text: JAPANESE INTERMEDIATE CODE: R313113 |
|
FPAY | Renewal fee payment (event date is renewal date of database) |
Free format text: PAYMENT UNTIL: 20130620 Year of fee payment: 5 |
|
R350 | Written notification of registration of transfer |
Free format text: JAPANESE INTERMEDIATE CODE: R350 |
|
LAPS | Cancellation because of no payment of annual fees |