The invention concerns compounds of formula (I) wherein W can represent a -(CH¿2?)¿2?-, -(CH¿2?)-C$m(Z)C- or -CH¿2?-CH=CH- group; R¿2? can in particular represent a piperidinyl group, a 1,2,3,6-tetrahydropyridinyl group optionally substituted, a hexahydro-1(H)-azepinyl group, a piperazinyl group optionally substituted...
The invention concerns N-piperidino-5-(4-bromophenyl)-1-(2,4dichlorophenyl)-4-ethylpyrazole-3-carboxamide, the salts and solvents thereof which are powerful antagonists of cannabinoid CB1? receptors. The method for preparing them consists in reacting a functional derivative of 5-(4-bromophenyl)-1-(2,4-dichlorophenyl)-...
The invention relates to compounds of formula (I) and to the salts thereof with mineral or organic acids, the solvates and/or hydrates thereof, exhibiting a high affinity and high selectivity with respect to human NK¿1? receptors of substance P. The invention also relates to a method for the production thereof, interm...
The invention concerns a method for preparing 5-(1-methylethyl)-6-(phenylmethyl)pyrimidine-2,4(1$i(H),3$i(H))-dione of formula (I) useful as synthesis intermediate for compounds of formula (II) wherein: A represents a RaOCH(Rb)-group, where Ra is a C¿1?-C¿6? alkyl group and Rb is a C¿1?-C¿4? alkyl group or a hydrogen ...
The invention relates to the use of a central cannabinoid receptor antagonist, by itself or in association with a compound for regulating metabolic disorders, especially a ß3-adrenergic receptor agonist, for the preparation of drugs useful in the treatment of appetency disorders.
The present invention relates to a method of crystallizing a tetrahydro-pyridine derivative, to the novel crystalline forms thereby obtained and to a pharmaceutical composition in which said tetrahydropyridine derivative in a given crystalline form is present as the active principle.
The subject of the present invention is the preparation of the (R)-(-)-2-hydroxy-2-(2-chlorophenyl)acetic acid of the formula (I) by the resolution of the corresponding racemic compound by using the compounds of the general formula (II).
The invention relates to compounds having formula (I). Said compounds have an affinity for hradykinin receptors with a selectivity for B, receptors and they can he used to prepare medicaments that are intended to treat or prevent persistent or chronic inflammatory diseases anil inflammation pathologies.
...
The invention relates to a microparticulate form of l-[2-(naphth-2-yl)ethyl]-4-(3-trifluoromethylphenyl)-l,2,3,6-tetrahydropyridine hydrochloride consisting of particles for which at least 55% of the population have a diameter below 50 micrometers, and to pharmaceutical compositions in which it is present.
...
The invention concerns antipsychotic compounds of formula (I) wherein: A represents a group selected among the following: -C$m(Z)C-; -CH=CH-; -CH¿2?-CH¿2?-; n is equal to 1 or 2; X represents a hydrogen, chlorine or fluorine atom, a methyl or methoxy group; Y represents a hydrogen atom or a chlorine or a fluorine atom...
The invention relates to a process for the preparation of a compound of formula (I) and the salts thereof by reacting the compound of formula (II) with the compound of formula (III), which comprises carrying out the reaction in dimethyl sulfoxide, at a temperature between 10 °C and 40 °C, preferably at room temperatur...
The present invention relates to a novel process for preparing (R)-(+)-3-{1-[2-(4-benzoyl-2-(3,4-difluorophenyl)morpholin-2-yl)ethyl]-4-phenylpiperid-4-yl}-l, 1-dimethylurea and the salts, solvates and/or hydrates thereof.
(R)-(+)-3-{l-[2-(4-Benzoyl-2-(3,4-
difluorophenyl)morpholin-2-yl)ethyl]-4-phenylpiperid-4-
yl}-l...
The present invention relates to a stable pharmaceutical composition for the oral administration of olanzapine that comprises olanzapine Form 1 or one of its pharmaceutically acceptable salts thereof, as active ingredient, which are stable to discoloration, degradation and exhibits dose uniformity.
...
The invention relates to the B form of ethyl [(7S) 7-[(2R) 2-(3-chlorophenyl)-2-hydroxyethylamino]-5,6,7,8-tetrahydronaphthalen-2-yloxy] acetate chlorohydrate, applicable as a medicament, with the following particular physical characteristics: characteristic IR absorption peaks (cm?-1¿): 2780, 2736, 1722, 1211; meltin...
A method for preparing dronedarone, characterized in that:
a) 2-butyl-5-nitrobenzofuran is hydrogenated in the presence of an appropriate
catalyst, to form 5-amino-2-butylbenzofuran,
b) the compound thus obtained is reacted with methanesulfonyl chloride or
methanesulfonic anhydride, the reaction taking place in the pr...
A method for preparing dronedarone, characterized in that, in an organic phase consisting of one or more solvents chosen from halogenated or nonhalogenated hydrocarbons, 2-butyl-5-(methanesulfonamido)bonzofuran is reacted with 4-[3-(dibutylamino)propoxy]benzoyl chloride hydrochloride, this being in the presence of a m...
A method for preparing dronedarone, characterized in that, in an organic phase consisting of one or more solvents chosen from halogenated or nonhalogenated hydrocarbons, 2-butyl-5-(methanesulfonamido)benzofuran is reacted with 4-[3-(dibutylamino)propoxy]benzoyl chloride hydrochloride, this being in the presence of a m...
The invention relates to a process for the preparation of a compound of formula (I) and the salts thereof by reacting the compound of formula (D) with the compound of formula (III), which comprises carrying out the reaction in dimethyl sulfoxide, at a temperature between 10 0C and 40 °C, preferably at room temper...
The invention relates to compounds of formula (I) and to the salts thereof with mineral or organic acids, the solvates and/or hydrates thereof, exhibiting a high affinity and high selectivity with respect to human NK¿1? receptors of substance P. The invention also relates to a method for the production thereof, interm...
The invention concerns compounds of formula (I) wherein W can represent a -(CH¿2?)¿2?-, -(CH¿2?)-C$m(Z)C- or -CH¿2?-CH=CH- group; R¿2? can in particular represent a piperidinyl group, a 1,2,3,6-tetrahydropyridinyl group optionally substituted, a hexahydro-1(H)-azepinyl group, a piperazinyl group optionally substituted...
(57) The invcnlion concerns compounds of formula (I), as well as ihcir addition sails with mineral or organic acids, their solvaies and/or theit hydraics, having strong affinily both lor human NK2 receptors of neurokinin A and lor human NK3 receptors of neurokinin B and anlaeonisis of said receptors. The invcnlion ...
A pharmaceutical composition for the treatment of appetency disorders, comprising a CBi receptor antagonist selected among N-piperidmno-5-(4-chlorophenyl)-1 -(2,4- dichlorophenyl)-4-methylpyrazole-3-carboxamide, its pharmaceutically acceptable salts and of their solvates in combination with a pharmaceutical carrier ...
The process according to the invention relates to the proparation of 2 chloromethyl thiophene of the formula (I) During this process thiophene is chloromethylated in the presence of one or more compounds containing keto group and optionally it is transformed into the compound of the formula (II) Compound of...
The invention concerns novel indolin-2-one derivatives or formula (I), their preparation and pharmaceutical compositions containing them. Said compounds have an affinity for ocytocin receptors.
The invention concerns 2-butyl-3-(4-[3(dibutylamino)propoxy]benzoyl)-5-nitro-benzofuran hydrochloride, its preparation and its use as synthesis intermediate in particular for preparing 2-butyl-3-(4-[3-(dibutylamino)propoxy]benzoyl)-5-nitro-benzofuran which is itself intermediate for dronedarone.
...
The invention concerns 2-butyl-3-(4-[3(dibutylamino)propoxy]benzoyl)-5-nitro-benzofuran hydrochloride, its preparation and its use as synthesis intermediate in particular for preparing 2-butyl-3-(4-[3-(dibutylamino)propoxy]benzoyl)-5-nitro-benzofuran which is itself intermediate for dronedarone.
...
The invention concerns compounds of general formula (I) wherein: R¿1? represents a hydrogen atom, an alkyl, phenylalkyl, phenylhydroxyalkyl, furanylalkyl or furanylhydroxyalkyl group; R¿2? represents either a hydrogen or a halogen atom or a trifluoromethyl, cyano, hydroxy, nitro, acetyl, alkoxy, amino group of gener...
The present invention relates to compounds of formula (I) and their pharmaceutically acceptable salts, solvates, hydrates and polymorphs. These compounds are powerful and selective CCK1 receptor agonists.
The invention concerns a disposable injection device comprising a pre-filled syringe (1) provided with a front nozzle (1a) bearing an injection needle (2) protected with a protective cap (3), and a syringe body (7) housing said syringe. The invention is characterised in that said injection device comprises a hub (32),...
The present invention relates to compounds of general formula (I), wherein R4 and R5 stand for hydrogen atom or form together an 1,3-butadienyl group, optionally substituted by a methylenedioxy group or one or more straight or branched Cl-4 alkyl group, straight or branched Cl-4 alkoxy group, hydroxyl group or halog...
A process for the manufacture of drugs intended for the treatemt of obesity by using a reversible seleective inhibitor of monoamine oxidase A, reversible selective inhibitor of monoamine oxidase B or a reversible mixed inhibitor of monoamine oxidase4 A and B
The invention relates to the B form of ethyl [(7S) 7-[(2R) 2-(3-chlorophenyl)-2-hydroxyethylamino]-5,6,7,8-tetrahy-dronaphthalen-2-yloxy] acetate chlorohydrate, applicable as a medicament, with the following particular physical characteristics: characteristic IR absorption peaks (cm'1): 2780, 2736, 1722, 1211; melting...
A compound with the formula (I):
in which:
- R1 and R2 each represent, independently of one another, hydrogen or a (C1-C3)alkyl;
- or R1 and R2 together with the nitrogen atom to which they are bound constitute a heterocyclic radical selected from among: a pyrrolidin-1-yl, a piperidin-1-yl, a morpholin-4-yl
- or R1...
The invention concerns irbesartan form A having a modified crystalline habit such that length/width ratio ranges between 1:1 and 10:1, preferably between 1:1 and 5:1 and a method for preparing said crystalline habit. The method is characterised in that it consists in either subjecting a crystalline suspension of irbes...
The present invention relates to a freeze-dried foffilulation consisting of an amorphous phase and a crystalline phase, which is phaffilaceutically acceptable, comprising at least one nonprotein active ingredient, characterized in that it contains mannitol and alanine in a ratio R of between 0.1 and 1, R representin...
Synthetic polysaccarides. process for their preperation and pharmaceutical
compositions containing them
The present invention relates to synthetic polysaccharides comprising a region for binding to antithrombin III consisting of a sequence of five monosaccharides bearing in total two carboxylic acid functions and...
A process for producing crystalline form I of cabergoline, which process comprises crystallization of the desired form from a toluene/diethyl ether mixture comprising raw cabergoline, followed by recovery and drying of the resulting crystals. A new solvate form V of cabergoline, useful as an intermediate, is also pr...
A pharmaceutical composition for the treatment of appetency disorders, comprising a CB1 receptor antagonist selected among N-piperidmno-5-(4-chlorophenyl)-I-(2,4- dichlorophenyl)-4-methylpyrazole-3-carboxamide, its pharmaceutically acceptable salts and of their solvates in combination with a pharmaceutical carrier, ...
A process for producing crystalline form I of cabergoline, which process comprises crystallization of the desired form from a toluene/diethyl ether mixture comprising raw cabergoline, followed by recovery and drying of the resulting crystals. A new solvate form V of cabergoline, useful as an intermediate, is also pr...
The present invention relates to a pharma- ceutical composition containing:
(a) a thienopyridine derivative of formula
in which R is hydrogen or a (C1-C4)alkoxycarbonyl group, or one of its
pharmaceutically acceptable salts; and (b) an HMG-CoA reductase inhibitor.
THE PRESENY INVENTION RELATES TO A PHARMACEUTICAL MICROSPHERES, CONTAINING ,AS ACTIVE PRINCILPE A MIXTURE OF VAIPROIC ACID AND OF ONE OF ITS PHARMACEUTICALLY ACCEPTABLE SALTS IN COMBINATION WITH A MIXTRIX VEHICLE SELECTED FROM GLYCEROL ESTERS,HYDROGENATED OILS ESTERIFIED POLYETHYLENE GLYCOLS OR WAXSE AND THEIR MIXTU...
The pharmaceutical compositions for oral administration according to the invention contain 0.5% to 20% of N-piperidino-5-(4-chlorophenyl)-l-(2,4-dichlorophenyl)-4-methylpyrazole-3-carboxamide in microcrystalline form, and pharmaceutical excipients; they are formulated by wet granulation.
Pharmaceutical composition for gastric
residence, characterized in that it comprises:
(a) an active principle consisting of a benzamide or a
benzamide salt,
(b) a carbon dioxide generator system, and
(c) a means allowing the partial retention of the
carbon dioxide generated by the said carbon dioxide
generator system....
3-(Pyrrolidin-3-yl)-1,3,4-oxadiazol-2(3h)-one
derivatives, their preparation and
their therapeutic application
Compounds corresponding to the general formula (I)
in which R1 represents hydrogen or an alkyl or
cycloalkylmethyl group, X1 represents hydrogen or a
halogen or an alkoxy group, or alternatively OR1 and X1
...
The present invention relates to an aqueous solution containing 1-[2-(2-naphthyl)ethyl]-4-(3-trifluoromethylphenyl)-1,2,3,6-tetrahydropyridine hydrochloride (hydrochloride of SR 57746), also comprising β-cyclodextrin (β-CD) and a pharmaceutically acceptable acid or buffer to give a pH of less than or equal to 3.
...
The invention concerns compounds derived from titanium of formula [TiFxLy] wherein L represents a compound of formula (II): wherein m is 0 or 1 and n is 0, 1 or 2, and x represents 2, 4 or 5, y represents 1 or 2 and z represents 0, 1 or 2. The invention also concerns the use of said compounds in compositions for oral ...
The invention concerns novel benzofuran or benzothiophene derivatives of general formula (I). Said compounds are useful as medicines in particular for treating pathological syndromes of the cardiovascular system.
Compounds of he general formula (I) wherein
R1 is methyl, ethyl or 2-morpholino-ehtyl-group;
R2 is piperidino, moorpholino or 4-methyl-piperazinyl group;
n is 2 or 3-
and their salts, solvates and hydrates.
The invention concerns 2-butyl-3-(4-[3(dibutylamirio)propoxy]benzoyl)-5-nitro-benzofuran hydrochloride, its preparation and its use as synthesis intermediate in particular for prepiring 2-butyl-3-(4-[3-(dibutylamino)propoxy)beni!:oyl)-5-ni-tro-ben/ot'uran which is itself intermediate for dronedarone.
...
The invention concerns 2-butyl-5-methanesulphonamido-benzofuran, its preparation and its use. Said compound is a synthesis intermediate in particular for preparing dronedarone.
The invention concerns compounds of formula (I), wherein: A is a group of formula (a) or (b), their salts or solvates, pharmaceutical compositions containing them, a method for preparing them and intermediates used in said method. The compounds of formula (I) can be prescribed for treating gastro-intestinal diseases ...
The invention concerns a pharmaceutical composition for parenteral administration, characterised in that it comprises: dronedarone or one of its pharmaceutically acceptable salts as active principle; a physiologically acceptable buffer solution capable of maintaining the pH of the composition between 3 and 5; a phys...
The invention concerns compounds of formula (I), as well as their addition salts with acids or organic salts, their solvates and/or hydrate(s), exhibiting affinity and selectivity for arginine-vasopressin V1b receptors and/or for ocytocin receptors, and further, for certain compounds an affinity for Vla receptors. ...
The invention concerns a method
for preparing a 4-alkoxycarbonylamino-l-ben-
zy]-4-phenylpiperidine of formula (I) by hydrolysis of l-benzy-4-cyano-4-phenylpiperidine (II) in acid medium (I) and treatment with bromine in the presence of an alkaline alcoholate. The invention also concern...
The invention concerns compounds of formula (I), and their preparation and pharmaceutical compositions containing them. Said compounds are CB2 cannabinoid receptor agonists.
The invention concerns compounds of formula (I), as well as their addition salts with mineral or organic acids, their solvates and/or their hydrates, having strong affinity both for human NK¿2? receptors of neurokinin A and for human NK¿3? receptors of neurokinin B and antagonists of said receptors. The invention al...
The invention relates to a formulation of N-[ll-[[2-(diethy]arnino)ethyl]amino]-7-methoxy-9-oxothioxanthen-4-yl]-methyl]formamide, or a pharmaceutically acceptable acid-addition salt thereof, and to the method of use thereof in the treatment of tumors and cancers.
The present invention relates to a convenient and stable bi-layer oral tablet formulation of cyclophosphamide and capecitabine. The methods of preparation of these formulations are described herein. Moreover, such formulations are useful for metronomic administration to treat cancer, e.g., breast cancer.
...
A method for preparing a compound characterized in that
(a)the compound of formula (II):
in which A and Ri, are defined as in claim 1, is reacted with a functional derivative of the acid of formula (III):
HOOG
*2 R.
in which R2, R3, R4, R5, n and x are as defined in claim 1,
(b) the carbonyl group of th...
A compound of formula (I) or a prodrug thereof, being a compound of formula I in which the amino group of the amidino-moiety is protected by hydroxy or a (l-6C)alkoxycarbonyl group. The invention also relates to a process for the preparation of the same.
The present invention relates to benzimidazole derivatives,to their preparation and to their therapeutic application.
The present invention relates to compounds corresponding to formula(I):
Cyclohexyl(alkyl)-propanolamines compound of formula (I):in whichA is a group of formula (a) or (b)whereR, R1, R2, R3, R4 and R5 are described as in the specification.
A pyrimidone derivative represented by formula (I) or a salt thereof, or a solvate thereof or a hydrate thereof having inhibitory activity against tau protein kinase 1: wherein R1 represents a C1-C12 alkyl group which may be substituted;R represents, for example, a group represented by the ...
Compounds, in racemic form or in the form of a pure enantiomer, of formula: 5 #a-2) in which- Ri and R2, which may be identical or different, each 10 independently represent a halogen atom; a hydroxy(Ci-C5)alkyl; a (C^-Cs) alkyl; an aralkyl in which the aryl...
A process for the preparation of methyl-[2(2-thienyl)-ethylamino]-(2-halogenophenyl)-acetates of general formula (VI) starting from the acetamides of general formula (VII). There are valuable pharmaceutically active ingredients of antithrombotic effect among the compounds of general formula (VI).
wherein R1I is (1-4C)alkoxy; R 2, R 3 and R 4 are independently (1-4C)alkoxy or 0S03-; the total number of sulfate groups is 4, 5 or 6; and the twisted lines represent bonds either above or below the plane of the six-membered ring to which they are attached; or a pharmaceutically acceptable salt thereof
Compounds of general formula (I)in which U represents a group of general formula (A) orin which formulae V represents a hydrogen or halogenatom, a (C1-C3)alkyl group or one or two (C1-C3) alkoxygroups, W and X each represent, respectively, eithertwo oxygen atoms, or an oxygen at...
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[Class : 5] Pharmaceutical And Hygienic Preparations, Medicated Soaps, Antiseptic Preparations, External Use In Dermatology And In Gynaecology Included In Class 5.
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[Class : 41] Organization Of Seminars, Working Groups, Search Groups And Congresses, In The Medical Field, Publishing Of Periodicals, Books, Guides, In The Medical Field. Assistance To Searchers, Medical Documentation Loan.[Class : 42] Assistance Of Searchers, Loan Or Renting Services Of Laboratory Equipment. Search In The Medical Field. Provision Of Temporary Offices.
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[Class : 5] Pharmaceutical And Veterinary Preparations, Sanitary Preparations For Medical Purposes, Dietetic Substances Adapted For Medicla Use, Food For Babies, Plasters, Materials For Dressings, Material For Stopping Teeth, Dental Wax, Disinfectants, Preparation For Destroying Vermin, Fungicides, Herbicides.
[Class : 16] Paper, Cardboard, Articles Of Paper Or Cardboard Namely, Cardboard Boxes, Bags, Sachets, Envelopes, Small Packets For Wrapping, All In Paper, Labels, Printed Matter, Newspapers And Periodicals, Books, Material For Teaching (Except Apparatus) Included In Class 16.
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[Class : 31] Agricultural, Horticultural And Forestry Products And Grains Not Included In Other Classes; Live Animals; Fresh Fruits And Vegetables; Seeds, Natural Plants And Flowers; Foodstuffs For Animals, Malt
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[Class : 9] Auio Video Compact Disks,Digital Optical Disks,Optical Computer Disks,Cd Roms, Computer Programmes, All These Goods For Use In The Pharmaceutical Field,Non Of The Aforesaid Goods Relating To Epicentres And/Or Seismology
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[Class : 16] Paper And Cardboard (Unprocessed,Semi Processed Or For Stationery Or Printing Purposes), Non Textile Labels,Adhesive (For Stationery Or Household Use),Cardboard Articles, Books,Printed Mattetr,Manuals,Pamphlets,Newspapers And Periodicals,Packaging Paper , Paper Or Plastic Packaging Bags, Sachets, Envelopes,Small Bags And Sheets,Instructional And Teaching Mate...
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["Trade mark is likely to be removed due to non filing of Renewal request within prescribed time limit In case of any discripancy contact respective TM Registry. "]
[Class : 1] Chemicals Used In Industry, Science And Photography, As Well As In Agriculture, Horticulture And Forestry; Unprocesed Artificial Resins, Unprocessed Plastics; Manures Fire Extinguishing Compositions, Tempering And Soldering Preparations; Chemical Substances For Preserving Foodstuffs; Tanning Substances Adhesives Used In Industry.
["Trade mark is likely to be removed due to non filing of Renewal request within prescribed time limit In case of any discripancy contact respective TM Registry. "]
[Class : 5] Pharmaceutical Products Included In Class 5.
["Trade mark is likely to be removed due to non filing of Renewal request within prescribed time limit In case of any discripancy contact respective TM Registry. "]
[Class : 31] Agricultural, Horticultural And Forestry Products And Grains Not Included In Other Classes; Live Animals; Fresh Fruits And Vegetables; Seeds, Natural Plants And Flowers, Foodstuffs For Animals, Malt.
["Trade mark is likely to be removed due to non filing of Renewal request within prescribed time limit In case of any discripancy contact respective TM Registry. "]
[Class : 5] Pharmaceutical, Veterinary And Sanitary Preparations; Dietetic Substances Adapted For Medical Use Food For Babies; Plasters, Materials For Dressings; Material For Stopping Teeth, Dental Wax; Disinfections; Preparation For Destroying Verin; Fungicides, Herbicides.
["Trade mark is likely to be removed due to non filing of Renewal request within prescribed time limit In case of any discripancy contact respective TM Registry. "]
["Trade mark is likely to be removed due to non filing of Renewal request within prescribed time limit In case of any discripancy contact respective TM Registry. "]
[Class : 5] Pharmaceuticals, Veterinary And Sanitary Preparations, Dietetic Substances Adapted For Medical Use, Food For Babies; Plasters, Materials For Dressings; Materials For Stopping Teeth, Dental Wax, Disinfectants, Preparation For Destroying Vermin; Fungicides, Herbicides.
[Class : 5] Pharmaceutical Products Included In Class 5.
["Trade mark is likely to be removed due to non filing of Renewal request within prescribed time limit In case of any discripancy contact respective TM Registry. "]
[Class : 5] Pharmaceutical Products Included In Class 5.
["Trade mark is likely to be removed due to non filing of Renewal request within prescribed time limit In case of any discripancy contact respective TM Registry. "]
["Trade mark is likely to be removed due to non filing of Renewal request within prescribed time limit In case of any discripancy contact respective TM Registry. "]
["Trade mark is likely to be removed due to non filing of Renewal request within prescribed time limit In case of any discripancy contact respective TM Registry. "]
[Class : 31] Agricultural, Horicultural And Foresty Products And Grains Not Included In Other Classes; Live Animals; Fresh Fruits And Vegetables; Seeds, Natural Plants And Flowers; Foodstuffs For Animals, Malt.
[Class : 5] Manufacturers And Trading In Pharmaceutical, Veterinary And Sanitary Preparations; Dietetic Substances Adapted For Medical Use Food For Babies; Plasters, Materials For Dressing; Materials, For Stopping Teeth, Dental Wax; Disinfections; Preparation For Destroying Vermin; Fungicides, Herbicides.
["Trade mark is likely to be removed due to non filing of Renewal request within prescribed time limit In case of any discripancy contact respective TM Registry. "]
[Class : 5] Pharmaceutical, And Veterinary Preparations; Sanitary Preparations For Medical Purposes; Dietetic Substances Adapted For Medical Use, Food For Babies; Plasters, Materials For Dressings; Materials For Stopping Teeth, Dental Wax; Disinfectants; Preparation For Destroying Vermin; Fungicides, Herbicides
[Class : 31] Agricultural, Horticultural And Forestry Products And Grains Not Included In Other Classes; Live Animals; Fresh Fruits And Vegetables; Seeds. Natural Plants And Flowers; Foodstuffs For Animals, Malt
["Trade mark is likely to be removed due to non filing of Renewal request within prescribed time limit In case of any discripancy contact respective TM Registry. "]
["Trade mark is likely to be removed due to non filing of Renewal request within prescribed time limit In case of any discripancy contact respective TM Registry. "]
[Class : 5] Pharmaceutical Products For The Central Nervous System Included In Class 5.
["Trade mark is likely to be removed due to non filing of Renewal request within prescribed time limit In case of any discripancy contact respective TM Registry. "]
[Class : 5] Medicinal And Pharmaceutical Preparations, Especially Pharmaceutical Preparations For Preventing And Treating Central Nervous System Discorders.
[Class : 16] Paper, Cardboard, Articles Of Paper Or Cardboard Namely; Cardboard Boxes, Bags, Sachets, Envelopes, Small Packets For Wrapping, All In Paper, Labels, Printed Matters, Newspapers And Periodicals, Books, Material For Teaching ( Except Apparatus).
["Trade mark is likely to be removed due to non filing of Renewal request within prescribed time limit In case of any discripancy contact respective TM Registry. "]
["Trade mark is likely to be removed due to non filing of Renewal request within prescribed time limit In case of any discripancy contact respective TM Registry. "]
[Class : 31] Agfricultural, Horticultural, Horticultural And Forestry Products And Grains Not Included In Other Classes; Live Animals ; Fresh Fruits And Vegetables; Seeds. Natural Plants And Flowers; Foodstuffs For Animals, Malt,
["Trade mark is likely to be removed due to non filing of Renewal request within prescribed time limit In case of any discripancy contact respective TM Registry. "]
[Class : 31] Agricultural, Horticultural And Forestry Products And Grains Not Included In Other Classes; Live Animals; Fresh Fruits And Vegetables; Seeds, Natural Plants And Flowers, Foodstuffs For Animals, Malt.
["Trade mark is likely to be removed due to non filing of Renewal request within prescribed time limit In case of any discripancy contact respective TM Registry. "]