ES2171991T3 - Forma galenica de liberacion prolongada de milnacipran. - Google Patents
Forma galenica de liberacion prolongada de milnacipran.Info
- Publication number
- ES2171991T3 ES2171991T3 ES97938949T ES97938949T ES2171991T3 ES 2171991 T3 ES2171991 T3 ES 2171991T3 ES 97938949 T ES97938949 T ES 97938949T ES 97938949 T ES97938949 T ES 97938949T ES 2171991 T3 ES2171991 T3 ES 2171991T3
- Authority
- ES
- Spain
- Prior art keywords
- hours
- milnacipran
- mum
- dose released
- dose
- 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.)
- Expired - Lifetime
Links
- GJJFMKBJSRMPLA-HIFRSBDPSA-N (1R,2S)-2-(aminomethyl)-N,N-diethyl-1-phenyl-1-cyclopropanecarboxamide Chemical compound C=1C=CC=CC=1[C@@]1(C(=O)N(CC)CC)C[C@@H]1CN GJJFMKBJSRMPLA-HIFRSBDPSA-N 0.000 title abstract 3
- 229960000600 milnacipran Drugs 0.000 title abstract 3
- 230000002035 prolonged effect Effects 0.000 title abstract 2
- 239000008194 pharmaceutical composition Substances 0.000 abstract 2
- 229920002472 Starch Chemical class 0.000 abstract 1
- CZMRCDWAGMRECN-UGDNZRGBSA-N Sucrose Chemical class O[C@H]1[C@H](O)[C@@H](CO)O[C@@]1(CO)O[C@@H]1[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO)O1 CZMRCDWAGMRECN-UGDNZRGBSA-N 0.000 abstract 1
- 229930006000 Sucrose Natural products 0.000 abstract 1
- 239000011230 binding agent Substances 0.000 abstract 1
- 235000013681 dietary sucrose Nutrition 0.000 abstract 1
- 238000000338 in vitro Methods 0.000 abstract 1
- 239000007788 liquid Substances 0.000 abstract 1
- 239000004531 microgranule Substances 0.000 abstract 1
- 239000004005 microsphere Substances 0.000 abstract 1
- 229920000642 polymer Polymers 0.000 abstract 1
- 239000008107 starch Chemical class 0.000 abstract 1
- 235000019698 starch Nutrition 0.000 abstract 1
- 229960004793 sucrose Drugs 0.000 abstract 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract 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
- A61K9/48—Preparations in capsules, e.g. of gelatin, of chocolate
- A61K9/50—Microcapsules having a gas, liquid or semi-solid filling; Solid microparticles or pellets surrounded by a distinct coating layer, e.g. coated microspheres, coated drug crystals
- A61K9/5073—Microcapsules having a gas, liquid or semi-solid filling; Solid microparticles or pellets surrounded by a distinct coating layer, e.g. coated microspheres, coated drug crystals having two or more different coatings optionally including drug-containing subcoatings
- A61K9/5078—Microcapsules having a gas, liquid or semi-solid filling; Solid microparticles or pellets surrounded by a distinct coating layer, e.g. coated microspheres, coated drug crystals having two or more different coatings optionally including drug-containing subcoatings with drug-free core
-
- 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
- A61K31/16—Amides, e.g. hydroxamic acids
- A61K31/165—Amides, e.g. hydroxamic acids having aromatic rings, e.g. colchicine, atenolol, progabide
-
- 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
- A61K9/14—Particulate form, e.g. powders, Processes for size reducing of pure drugs or the resulting products, Pure drug nanoparticles
- A61K9/16—Agglomerates; Granulates; Microbeadlets ; Microspheres; Pellets; Solid products obtained by spray drying, spray freeze drying, spray congealing,(multiple) emulsion solvent evaporation or extraction
- A61K9/1605—Excipients; Inactive ingredients
- A61K9/1629—Organic macromolecular compounds
- A61K9/1652—Polysaccharides, e.g. alginate, cellulose derivatives; Cyclodextrin
-
- 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
- A61K9/14—Particulate form, e.g. powders, Processes for size reducing of pure drugs or the resulting products, Pure drug nanoparticles
- A61K9/16—Agglomerates; Granulates; Microbeadlets ; Microspheres; Pellets; Solid products obtained by spray drying, spray freeze drying, spray congealing,(multiple) emulsion solvent evaporation or extraction
- A61K9/167—Agglomerates; Granulates; Microbeadlets ; Microspheres; Pellets; Solid products obtained by spray drying, spray freeze drying, spray congealing,(multiple) emulsion solvent evaporation or extraction with an outer layer or coating comprising drug; with chemically bound drugs or non-active substances on their surface
- A61K9/1676—Agglomerates; Granulates; Microbeadlets ; Microspheres; Pellets; Solid products obtained by spray drying, spray freeze drying, spray congealing,(multiple) emulsion solvent evaporation or extraction with an outer layer or coating comprising drug; with chemically bound drugs or non-active substances on their surface having a drug-free core with discrete complete coating layer containing drug
-
- 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
- A61K9/48—Preparations in capsules, e.g. of gelatin, of chocolate
- A61K9/50—Microcapsules having a gas, liquid or semi-solid filling; Solid microparticles or pellets surrounded by a distinct coating layer, e.g. coated microspheres, coated drug crystals
- A61K9/5005—Wall or coating material
- A61K9/5021—Organic macromolecular compounds
- A61K9/5036—Polysaccharides, e.g. gums, alginate; Cyclodextrin
- A61K9/5042—Cellulose; Cellulose derivatives, e.g. phthalate or acetate succinate esters of hydroxypropyl methylcellulose
- A61K9/5047—Cellulose ethers containing no ester groups, e.g. hydroxypropyl methylcellulose
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/24—Antidepressants
Landscapes
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Epidemiology (AREA)
- Biomedical Technology (AREA)
- Psychiatry (AREA)
- Pain & Pain Management (AREA)
- Neurology (AREA)
- Neurosurgery (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Organic Chemistry (AREA)
- Medicinal Preparation (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Medicines Containing Antibodies Or Antigens For Use As Internal Diagnostic Agents (AREA)
- Electrochromic Elements, Electrophoresis, Or Variable Reflection Or Absorption Elements (AREA)
- Polishing Bodies And Polishing Tools (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Orthopedics, Nursing, And Contraception (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Medicines Containing Plant Substances (AREA)
Abstract
EL OBJETO DE LA PRESENTE INVENCION SE REFIERE UNA FORMA GALENICA CON LIBERACION PROLONGADA, DESTINADA A LA ADMINISTRACION POR VIA ORAL DE UNA SOLA DOSIS DIARIA DE ENTRE 60 Y 140 MG DE MILNACIPRANO QUE SE PRESENTA CON UNA FORMA MULTIPARTICULAR, QUE REUNE VARIOS MINIGRANULOS QUE COMPRENDE CADA UNO UNA MINIESFERA ACTIVA QUE COMPRENDE UN NUCLEO DE SACAROSA Y/O DE ALMIDON DE GRANULOMETRIA COMPRENDIDA ENTRE 200 Y 2000 MI M Y QUE CONTIENE ENTRE 150 Y 1000 MI G DE MILNACIPRANO ASI COMO UN AGENTE AGLOMERANTE, ESTANDO CADA MICROGRANULO REVESTIDO POR UNA PELICULA, CON BASE DE AL MENOS UN POLIMERO NO HIDROSOLUBLE PERO PERMEABLE A LOS LIQUIDOS FISIOLOGICOS, DE ESPESOR COMPRENDIDO ENTRE 20 Y 00 MI M, PERMITIENDO DICHA FORMA GALENICA UNA LIBERACION IN VITRO QUE CORRESPONDE AL PERFIL SEGUN ENTRE UN 10 Y UN 55 % DE LA DOSIS LIBERADA EN DOS HORAS, ENTRE UN 40 Y UN 75 % DE LA DOSIS LIBERADA EN 4 HORAS, ENTRE UN 70 Y UN 90 % DE LA DOSIS LIBERADA EN 8 HORAS, ENTRE UN 80 Y UN 100 % DE LA DOSIS LIBERADA EN 12 HORAS.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| FR9610528A FR2752732B1 (fr) | 1996-08-28 | 1996-08-28 | Forme galenique a liberation prolongee de milnacipran |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ES2171991T3 true ES2171991T3 (es) | 2002-09-16 |
Family
ID=9495256
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ES97938949T Expired - Lifetime ES2171991T3 (es) | 1996-08-28 | 1997-08-26 | Forma galenica de liberacion prolongada de milnacipran. |
Country Status (14)
| Country | Link |
|---|---|
| US (1) | US6699506B1 (es) |
| EP (1) | EP0939626B1 (es) |
| JP (2) | JP4549442B2 (es) |
| CN (1) | CN1108791C (es) |
| AT (1) | ATE213629T1 (es) |
| AU (1) | AU727018B2 (es) |
| BR (1) | BR9711378A (es) |
| CA (1) | CA2264238C (es) |
| DE (1) | DE69710757T2 (es) |
| DK (1) | DK0939626T3 (es) |
| ES (1) | ES2171991T3 (es) |
| FR (1) | FR2752732B1 (es) |
| PT (1) | PT939626E (es) |
| WO (1) | WO1998008495A1 (es) |
Families Citing this family (41)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE19928312A1 (de) * | 1999-06-16 | 2000-12-21 | Schering Ag | Arzneimittelzubereitung mit verzögerter Wirkstoffabgabe |
| FR2830447B1 (fr) * | 2001-10-09 | 2004-04-16 | Flamel Tech Sa | Forme galenique orale microparticulaire pour la liberation retardee et controlee de principes actifs pharmaceutiques |
| US8101209B2 (en) * | 2001-10-09 | 2012-01-24 | Flamel Technologies | Microparticulate oral galenical form for the delayed and controlled release of pharmaceutical active principles |
| US6635675B2 (en) * | 2001-11-05 | 2003-10-21 | Cypress Bioscience, Inc. | Method of treating chronic fatigue syndrome |
| US6602911B2 (en) | 2001-11-05 | 2003-08-05 | Cypress Bioscience, Inc. | Methods of treating fibromyalgia |
| AU2003246791A1 (en) * | 2002-04-09 | 2003-10-20 | Flamel Technologies | Oral suspension of amoxicillin capsules |
| JP4732696B2 (ja) | 2002-04-09 | 2011-07-27 | フラメル・テクノロジー | 活性成分の改変された放出のための、マイクロカプセルの水性懸濁液形態での経口医薬品製剤 |
| US20060003004A1 (en) * | 2002-10-25 | 2006-01-05 | Collegium Pharmaceutical, Inc. | Pulsatile release compositions of milnacipran |
| US20060024366A1 (en) * | 2002-10-25 | 2006-02-02 | Collegium Pharmaceutical, Inc. | Modified release compositions of milnacipran |
| WO2004039361A1 (en) * | 2002-10-25 | 2004-05-13 | Collegium Pharmaceutical, Inc. | Pulsatile release compositions of milnacipran |
| US20040132826A1 (en) * | 2002-10-25 | 2004-07-08 | Collegium Pharmaceutical, Inc. | Modified release compositions of milnacipran |
| US7704527B2 (en) | 2002-10-25 | 2010-04-27 | Collegium Pharmaceutical, Inc. | Modified release compositions of milnacipran |
| MXPA05008033A (es) * | 2003-01-28 | 2006-04-28 | Collegium Pharmaceutical Inc | Composiciones de milnacipran en forma de multiparticulas para administracion oral. |
| FR2851163B1 (fr) | 2003-02-14 | 2007-04-27 | Utilisation de l'enantiomere dextrogyre du milnacipran pour la preparation d'un medicament | |
| NZ541733A (en) | 2003-02-14 | 2009-03-31 | Pf Medicament | Use of the enantiomer (1S,2R) of milnacipran for the preparation of a medicament |
| EP1894565B1 (en) | 2005-06-10 | 2013-10-30 | Pierre Fabre Médicament S.A. | Stabilized milnacipran formulation |
| US7994220B2 (en) | 2005-09-28 | 2011-08-09 | Cypress Bioscience, Inc. | Milnacipran for the long-term treatment of fibromyalgia syndrome |
| US20080319083A1 (en) * | 2006-01-27 | 2008-12-25 | Asahi Kasei Pharma Corporation | Medicine for transnasal administration |
| JP5452236B2 (ja) * | 2007-03-02 | 2014-03-26 | ファーナム・カンパニーズ・インコーポレーテッド | ロウ様物質を用いた徐放性組成物 |
| CN101301283B (zh) * | 2007-05-10 | 2011-04-06 | 上海医药工业研究院 | 一种米那普仑的经鼻脑转运组合物 |
| EP2110129A1 (en) | 2008-04-18 | 2009-10-21 | Pierre Fabre Medicament | Use of enantiomer (1S, 2R) milnacipran hydrochloride for the preventive treatment of suicidal behaviour in depressed patients |
| ES2536736T3 (es) * | 2008-09-04 | 2015-05-28 | Farnam Companies, Inc. | Formulaciones masticables de liberación sostenida |
| DK3045043T3 (da) | 2009-02-26 | 2020-08-03 | Relmada Therapeutics Inc | Orale farmaceutiske sammensætninger af 3-hydroxy-n-methylmorphinan med forlænget frigivelse og fremgangsmåde til anvendelse |
| US20100239681A1 (en) * | 2009-03-20 | 2010-09-23 | Biokey, Inc. | Controlled Release Particulates Containing Water-Insoluble Drug |
| FR2943546A1 (fr) * | 2009-03-31 | 2010-10-01 | Nouveaux Produits Pharma Sas | Excipient pharmaceutique fonctionnalise ameliorant la biodisponibilite de substances actives peu solubles, microgranules l'incorporant. |
| FR2945449B1 (fr) * | 2009-05-15 | 2012-10-05 | Pf Medicament | Procede d'impregnation par co2 supercritique |
| EP2461801A2 (en) | 2009-08-05 | 2012-06-13 | Lupin Limited | Controlled release pharmaceutical compositions of milnacipran |
| US8865937B2 (en) * | 2009-11-06 | 2014-10-21 | Mahendra G. Dedhiya | Crystalline forms of (1S,2R)-2-(amino methyl)-N,N-diethyl-1-phenyl cyclopropane carboxamide |
| WO2011088331A1 (en) * | 2010-01-14 | 2011-07-21 | Forest Laboratories Holdings Limited | Stable dosage forms of levomilnacipran |
| WO2011107921A2 (en) | 2010-03-04 | 2011-09-09 | Ranbaxy Laboratories Limited | Modified release composition of milnacipran |
| WO2011107922A2 (en) | 2010-03-04 | 2011-09-09 | Ranbaxy Laboratories Limited | Extended release composition of milnacipran |
| WO2012028922A2 (en) | 2010-08-30 | 2012-03-08 | Lupin Limited | Controlled release pharmaceutical compositions of milnacipran |
| FR2978350B1 (fr) | 2011-07-28 | 2013-11-08 | Pf Medicament | Medicament a base de levomilnacipran pour la rehabilitation fonctionnelle apres accident neurologique aigu |
| CN102793683B (zh) * | 2012-09-04 | 2013-04-17 | 海南康虹医药科技开发有限公司 | 一种含左旋米那普仑的缓释组合物及其制备方法 |
| US10835495B2 (en) | 2012-11-14 | 2020-11-17 | W. R. Grace & Co.-Conn. | Compositions containing a biologically active material and a non-ordered inorganic oxide material and methods of making and using the same |
| JP6186139B2 (ja) * | 2013-03-08 | 2017-08-23 | 杏林製薬株式会社 | 口腔内速崩壊性錠剤 |
| CN105769823A (zh) * | 2014-12-24 | 2016-07-20 | 上海星泰医药科技有限公司 | 一种左旋盐酸米那普仑缓释胶囊及其制备方法 |
| EP3167879A1 (en) * | 2015-11-10 | 2017-05-17 | Evonik Technochemie GmbH | Gastric retention active delivery systems |
| CN110711185A (zh) * | 2018-07-11 | 2020-01-21 | 北京万全德众医药生物技术有限公司 | 左旋米那普仑缓释胶囊 |
| JP7315383B2 (ja) * | 2019-06-27 | 2023-07-26 | 株式会社Screenホールディングス | インクジェット用水性組成物及び固体製剤 |
| CN114569566A (zh) * | 2020-12-02 | 2022-06-03 | 四川科瑞德制药股份有限公司 | 一种盐酸米那普仑制剂的制备方法 |
Family Cites Families (16)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR2508035A1 (fr) * | 1981-06-23 | 1982-12-24 | Fabre Sa Pierre | Derives d'aryl-1-aminomethyl-2 cyclopropanes carboxamides (z), leur preparation et leur application en tant que medicaments utiles dans le traitement des troubles du systeme nerveux central |
| JPS58180481A (ja) | 1982-04-15 | 1983-10-21 | Kyowa Hakko Kogyo Co Ltd | 新規なピペリジン誘導体 |
| FR2581060B1 (fr) * | 1985-04-25 | 1988-07-01 | Pf Medicament | Procede industriel d'obtention du midalcipran |
| FR2581059B1 (fr) * | 1985-04-25 | 1988-04-22 | Pf Medicament | Procede de preparation du chlorhydrate de phenyl-1 diethyl amino carbonyl-1 aminomethyl-2 cyclopropane (z) |
| US5026560A (en) * | 1987-01-29 | 1991-06-25 | Takeda Chemical Industries, Ltd. | Spherical granules having core and their production |
| FI95572C (fi) | 1987-06-22 | 1996-02-26 | Eisai Co Ltd | Menetelmä lääkeaineena käyttökelpoisen piperidiinijohdannaisten tai sen farmaseuttisen suolan valmistamiseksi |
| FR2640972B1 (es) * | 1988-12-28 | 1991-04-19 | Pf Medicament | |
| CA2007181C (en) * | 1989-01-06 | 1998-11-24 | Angelo Mario Morella | Sustained release pharmaceutical composition |
| JP2807577B2 (ja) | 1990-06-15 | 1998-10-08 | エーザイ株式会社 | 環状アミド誘導体 |
| FR2677019B1 (fr) | 1991-05-27 | 1994-11-25 | Pf Medicament | Nouvelles piperidines disubstituees-1,4, leur preparation et leur application en therapeutique. |
| GB9113872D0 (en) * | 1991-06-27 | 1991-08-14 | Sandoz Ag | Improvements in or relating to organic compounds |
| US5160742A (en) * | 1991-12-31 | 1992-11-03 | Abbott Laboratories | System for delivering an active substance for sustained release |
| DE69327583T2 (de) | 1992-03-31 | 2000-05-31 | Glaxo Group Ltd., Greenford | Substituierte phenylcarbamate und phenylharnstoffe, ihre herstellung und ihre verwendung als 5-ht4-antagonisten |
| US5578316A (en) * | 1992-06-04 | 1996-11-26 | Smithkline Beecham Corporation | Palatable pharmaceutical compositions |
| CA2134038C (en) * | 1994-06-16 | 1997-06-03 | David Taiwai Wong | Potentiation of drug response |
| US5910319A (en) * | 1997-05-29 | 1999-06-08 | Eli Lilly And Company | Fluoxetine enteric pellets and methods for their preparation and use |
-
1996
- 1996-08-28 FR FR9610528A patent/FR2752732B1/fr not_active Expired - Fee Related
-
1997
- 1997-08-26 AU AU41212/97A patent/AU727018B2/en not_active Expired
- 1997-08-26 EP EP97938949A patent/EP0939626B1/fr not_active Expired - Lifetime
- 1997-08-26 US US09/254,014 patent/US6699506B1/en not_active Expired - Lifetime
- 1997-08-26 CA CA002264238A patent/CA2264238C/fr not_active Expired - Lifetime
- 1997-08-26 JP JP51133798A patent/JP4549442B2/ja not_active Expired - Lifetime
- 1997-08-26 WO PCT/FR1997/001525 patent/WO1998008495A1/fr not_active Ceased
- 1997-08-26 PT PT97938949T patent/PT939626E/pt unknown
- 1997-08-26 AT AT97938949T patent/ATE213629T1/de active
- 1997-08-26 DK DK97938949T patent/DK0939626T3/da active
- 1997-08-26 ES ES97938949T patent/ES2171991T3/es not_active Expired - Lifetime
- 1997-08-26 DE DE69710757T patent/DE69710757T2/de not_active Expired - Lifetime
- 1997-08-26 BR BR9711378A patent/BR9711378A/pt not_active Application Discontinuation
- 1997-08-26 CN CN97198442A patent/CN1108791C/zh not_active Expired - Lifetime
-
2010
- 2010-03-10 JP JP2010053612A patent/JP5431214B2/ja not_active Expired - Lifetime
Also Published As
| Publication number | Publication date |
|---|---|
| EP0939626B1 (fr) | 2002-02-27 |
| BR9711378A (pt) | 1999-08-17 |
| US6699506B1 (en) | 2004-03-02 |
| JP2010163447A (ja) | 2010-07-29 |
| JP4549442B2 (ja) | 2010-09-22 |
| WO1998008495A1 (fr) | 1998-03-05 |
| DK0939626T3 (da) | 2002-05-27 |
| DE69710757D1 (de) | 2002-04-04 |
| FR2752732A1 (fr) | 1998-03-06 |
| DE69710757T2 (de) | 2004-11-04 |
| PT939626E (pt) | 2002-07-31 |
| CA2264238A1 (fr) | 1998-03-05 |
| CN1108791C (zh) | 2003-05-21 |
| JP2000516946A (ja) | 2000-12-19 |
| CA2264238C (fr) | 2009-02-24 |
| ATE213629T1 (de) | 2002-03-15 |
| AU727018B2 (en) | 2000-11-30 |
| CN1232387A (zh) | 1999-10-20 |
| FR2752732B1 (fr) | 1998-11-20 |
| JP5431214B2 (ja) | 2014-03-05 |
| AU4121297A (en) | 1998-03-19 |
| EP0939626A1 (fr) | 1999-09-08 |
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