ES2190241T3 - Compuestos farmaceuticos de liberacion rapida de substancias medicamentosas. - Google Patents
Compuestos farmaceuticos de liberacion rapida de substancias medicamentosas.Info
- Publication number
- ES2190241T3 ES2190241T3 ES99941418T ES99941418T ES2190241T3 ES 2190241 T3 ES2190241 T3 ES 2190241T3 ES 99941418 T ES99941418 T ES 99941418T ES 99941418 T ES99941418 T ES 99941418T ES 2190241 T3 ES2190241 T3 ES 2190241T3
- Authority
- ES
- Spain
- Prior art keywords
- composition
- powder
- active substance
- sieve
- therapeutically
- 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
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
- A61K9/20—Pills, tablets, discs, rods
- A61K9/2004—Excipients; Inactive ingredients
- A61K9/2009—Inorganic compounds
-
- 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
- A61K9/1611—Inorganic compounds
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
- A61P1/04—Drugs for disorders of the alimentary tract or the digestive system for ulcers, gastritis or reflux esophagitis, e.g. antacids, inhibitors of acid secretion, mucosal protectants
-
- 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
- A61P25/04—Centrally acting analgesics, e.g. opioids
-
- 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
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P5/00—Drugs for disorders of the endocrine system
- A61P5/38—Drugs for disorders of the endocrine system of the suprarenal hormones
- A61P5/46—Drugs for disorders of the endocrine system of the suprarenal hormones for decreasing, blocking or antagonising the activity of glucocorticosteroids
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Medicinal Chemistry (AREA)
- General Health & Medical Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Organic Chemistry (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Epidemiology (AREA)
- Inorganic Chemistry (AREA)
- Pain & Pain Management (AREA)
- Neurosurgery (AREA)
- Neurology (AREA)
- Biomedical Technology (AREA)
- Psychiatry (AREA)
- Rheumatology (AREA)
- Endocrinology (AREA)
- Diabetes (AREA)
- Medicinal Preparation (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Abstract
Compuesto farmacéutico de liberación rápida para administración oral, que comprende una substancia terapéutica y/o profilácticamente activa, cuya substancia activa queda definida por una de las características i) o ii): i) la substancia activa tiene una solubilidad máxima de 0, 1 % peso/volumen en ácido clorhídrico 0, 1 N a temperatura ambiente; ii) la substancia activa tiene un valor pKa máximo de 5, 5, y en el que el compuesto farmacéutico de liberación rápida tiene además una de las características iii) o iv): iv) el compuesto farmacéutico de liberación rápida se basa en un material en polvo que comprende la substancia terapéutica y/o profilácticamente activa y que tiene un tamaño de partículas que, cuando el material en polvo es sometido a análisis de cribado, como mínimo, 90 % peso/peso de las partículas atraviesan una criba de 180 µm, estableciendo contacto el material en polvo con un medio acuoso para formar un compuesto en partículas, que tiene un tamaño de partículas tal que, cuando el compuesto en partículas es sometido a análisis de cribado, entonces un mínimo de 50 % peso/peso de las partículas atraviesan una criba de 180 µm; iv) el compuesto farmacéutico de liberación rápida adopta la forma de compuesto en partículas o se basa en un compuesto en partículas, que es obtenido por contacto de un material en polvo que comprende la substancia terapéutica y/o profilácticamente activa con un medio acuoso de manera tal que el tamaño medio de partículas del compuesto es como máximo 100 % superior al tamaño medio de partículas del material en polvo antes de contacto con el medio acuoso, y en el que el compuesto farmacéutico de liberación rápida es tal que la substancia activa recibe el contacto de una substancia alcalina, y en el que el compuesto farmacéutico de liberación rápida, una vez comprobada de acuerdo con el método de disolución I que se ha definido utilizando ácido clorhídrico 0, 07 N como medio de disolución, libera un mínimo de 50 % peso/peso de la substancia activa dentro de los primeros 20 minutos de la prueba.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DKPA199801143 | 1998-09-10 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ES2190241T3 true ES2190241T3 (es) | 2003-07-16 |
Family
ID=8101500
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ES99941418T Expired - Lifetime ES2190241T3 (es) | 1998-09-10 | 1999-09-10 | Compuestos farmaceuticos de liberacion rapida de substancias medicamentosas. |
Country Status (13)
| Country | Link |
|---|---|
| US (1) | US6713089B1 (es) |
| EP (1) | EP1109534B1 (es) |
| JP (2) | JP5026635B2 (es) |
| AT (1) | ATE232382T1 (es) |
| AU (1) | AU5504599A (es) |
| CA (1) | CA2343148C (es) |
| DE (1) | DE69905380T2 (es) |
| DK (1) | DK1109534T3 (es) |
| EA (1) | EA004032B1 (es) |
| ES (1) | ES2190241T3 (es) |
| PT (1) | PT1109534E (es) |
| TR (1) | TR200100708T2 (es) |
| WO (1) | WO2000015195A1 (es) |
Families Citing this family (82)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6489346B1 (en) | 1996-01-04 | 2002-12-03 | The Curators Of The University Of Missouri | Substituted benzimidazole dosage forms and method of using same |
| US5840737A (en) | 1996-01-04 | 1998-11-24 | The Curators Of The University Of Missouri | Omeprazole solution and method for using same |
| US8231899B2 (en) * | 1998-09-10 | 2012-07-31 | Nycomed Danmark Aps | Quick release pharmaceutical compositions of drug substances |
| SA99191255B1 (ar) * | 1998-11-30 | 2006-11-25 | جي دي سيرل اند كو | مركبات سيليكوكسيب celecoxib |
| US20020035107A1 (en) | 2000-06-20 | 2002-03-21 | Stefan Henke | Highly concentrated stable meloxicam solutions |
| EP1250921A1 (en) * | 2001-04-21 | 2002-10-23 | BOEHRINGER INGELHEIM INTERNATIONAL GmbH | Fast disintegrating meloxicam tablet |
| US8206741B2 (en) | 2001-06-01 | 2012-06-26 | Pozen Inc. | Pharmaceutical compositions for the coordinated delivery of NSAIDs |
| DE10161077A1 (de) | 2001-12-12 | 2003-06-18 | Boehringer Ingelheim Vetmed | Hochkonzentrierte stabile Meloxicamlösungen zur nadellosen Injektion |
| US20030161875A1 (en) * | 2002-02-27 | 2003-08-28 | Deepak Murpani | Fast dissolving tablets of cyclooxygenase-2 enzyme inhibitors |
| US8992980B2 (en) | 2002-10-25 | 2015-03-31 | Boehringer Ingelheim Vetmedica Gmbh | Water-soluble meloxicam granules |
| US20040109889A1 (en) * | 2002-12-04 | 2004-06-10 | Bunick Frank J. | Surface treatment composition for soft substrates |
| US20040202717A1 (en) * | 2003-04-08 | 2004-10-14 | Mehta Atul M. | Abuse-resistant oral dosage forms and method of use thereof |
| WO2005004915A2 (en) * | 2003-07-09 | 2005-01-20 | Boehringer Ingelheim International Gmbh | Compositions comprising meloxicam |
| US8993599B2 (en) | 2003-07-18 | 2015-03-31 | Santarus, Inc. | Pharmaceutical formulations useful for inhibiting acid secretion and methods for making and using them |
| EP1568369A1 (en) | 2004-02-23 | 2005-08-31 | Boehringer Ingelheim Vetmedica Gmbh | Use of meloxicam for the treatment of respiratory diseases in pigs |
| US20050220877A1 (en) * | 2004-03-31 | 2005-10-06 | Patel Ashish A | Bilayer tablet comprising an antihistamine and a decongestant |
| US8906940B2 (en) | 2004-05-25 | 2014-12-09 | Santarus, Inc. | Pharmaceutical formulations useful for inhibiting acid secretion and methods for making and using them |
| PL1916994T3 (pl) * | 2004-06-29 | 2014-05-30 | Takeda Pharma As | Wytwarzanie kompozycji farmaceutycznej o szybkim uwalnianiu leków nierozpuszczalnych w wodzie i kompozycje farmaceutyczne otrzymywane sposobem według wynalazku |
| JP5490347B2 (ja) * | 2005-05-27 | 2014-05-14 | エスエス製薬株式会社 | 経口投与用製剤 |
| JO3352B1 (ar) | 2005-06-17 | 2019-03-13 | Apr Applied Pharma Res Sa | صيغ دايكلوفيناك وطرق استخدامه |
| AU2006271150A1 (en) | 2005-07-20 | 2007-01-25 | Panacea Biotec Ltd. | Novel pharmaceutical modified release dosage form cyclooxygenase enzyme inhibitor |
| CA2615063A1 (en) * | 2005-07-22 | 2007-02-01 | Myriad Genetics, Inc. | High drug load formulations and dosage forms |
| SG10202003901UA (en) | 2005-12-13 | 2020-05-28 | Incyte Holdings Corp | Heteroaryl substituted pyrrolo[2,3-b]pyridines and pyrrolo[2,3-b]pyrimidines as janus kinase inhibitors |
| EP1965774A2 (en) * | 2005-12-30 | 2008-09-10 | Cogentus Pharmaceuticals, Inc. | Oral pharmaceutical formulations containing non-steroidal anti-inflammatory drugs and acid inhibitors |
| WO2007130507A2 (en) * | 2006-05-03 | 2007-11-15 | Proethic Pharmaceuticals, Inc. | Acute pain medications based on fast acting diclofenac-opioid combinations |
| EP2043613A1 (en) * | 2006-07-14 | 2009-04-08 | Fmc Corporation | Solid form |
| WO2008062449A2 (en) * | 2006-09-18 | 2008-05-29 | Glenmark Pharmaceuticals Limited | A novel pharmaceutical soft gel composition containing dexibuprofen and paracetamol |
| US20080081067A1 (en) * | 2006-10-03 | 2008-04-03 | Gupta Manishkumar | Sustained release pharmaceutical compositions of venlafaxine and process for preparation thereof |
| US20080311162A1 (en) * | 2007-05-16 | 2008-12-18 | Olivia Darmuzey | Solid form |
| KR20150036210A (ko) | 2007-06-13 | 2015-04-07 | 인사이트 코포레이션 | 야누스 키나제 억제제(R)―3―(4―(7H―피롤로[2,3-d]피리미딘―4―일)―1H―피라졸―1―일)―3―사이클로펜틸프로판니트릴의 염 |
| ES2560899T3 (es) | 2007-09-14 | 2016-02-23 | Wockhardt Limited | Composiciones de diacereína |
| ES2590604T3 (es) * | 2008-01-04 | 2016-11-22 | Schabar Research Associates Llc | Composición que comprende un analgésico y un antihistamínico |
| JP5757864B2 (ja) | 2008-05-20 | 2015-08-05 | ニューロジェシックス, インコーポレイテッド | 水溶性アセトアミノフェン類似体 |
| EP2291084A4 (en) | 2008-05-20 | 2012-04-25 | Neurogesx Inc | CARBONATE PRODRUGS AND METHOD FOR THEIR USE |
| US9220698B2 (en) | 2008-09-09 | 2015-12-29 | Pozen Inc. | Method for delivering a pharmaceutical composition to patient in need thereof |
| SI2432472T1 (sl) | 2009-05-22 | 2019-11-29 | Incyte Holdings Corp | 3-(4-(7H-pirolo(2,3-d)pirimidin-4-il)-1H-pirazol-1-il)oktan- ali heptan-nitril kot inhibitorji JAK |
| EP2445344A4 (en) * | 2009-06-25 | 2013-01-23 | Pozen Inc | METHOD FOR THE TREATMENT OF A PATIENT REQUIRED BY ASPIRIN THERAPY |
| KR20120030106A (ko) | 2009-06-25 | 2012-03-27 | 아스트라제네카 아베 | Nsaid-연관된 궤양의 발생 위험이 있는 환자의 치료 방법 |
| TW201113285A (en) * | 2009-09-01 | 2011-04-16 | Incyte Corp | Heterocyclic derivatives of pyrazol-4-yl-pyrrolo[2,3-d]pyrimidines as janus kinase inhibitors |
| ES3037313T3 (en) | 2009-10-12 | 2025-09-30 | Boehringer Ingelheim Vetmedica Gmbh | Containers for compositions comprising meloxicam |
| MX2012010077A (es) | 2010-03-03 | 2012-09-12 | Boehringer Ingelheim Vetmed | Uso de meloxicam para el tratamiento a largo plazo de trastornos musculoesqueleticos en gatos. |
| EP3354652B1 (en) | 2010-03-10 | 2020-05-06 | Incyte Holdings Corporation | Piperidin-4-yl azetidine derivatives as jak1 inhibitors |
| US9795568B2 (en) | 2010-05-05 | 2017-10-24 | Boehringer Ingelheim Vetmedica Gmbh | Low concentration meloxicam tablets |
| PE20130216A1 (es) | 2010-05-21 | 2013-02-27 | Incyte Corp | Formulacion topica para un inhibidor de jak |
| EP2394641A1 (en) | 2010-05-30 | 2011-12-14 | Abdi Ibrahim Ilac Sanayi ve Ticaret Anonim Sirketi | Pharmaceutical formulations of lornoxicam |
| PE20140146A1 (es) | 2010-11-19 | 2014-02-06 | Incyte Corp | Derivados de pirrolopiridina y pirrolopirimidina sustituidos con ciclobutilo como inhibidores de jak |
| US9034884B2 (en) | 2010-11-19 | 2015-05-19 | Incyte Corporation | Heterocyclic-substituted pyrrolopyridines and pyrrolopyrimidines as JAK inhibitors |
| WO2012146314A1 (en) | 2011-04-29 | 2012-11-01 | Refarmed Chemicals Sa | Thin gelatin capsules for rapid drug release in the mouth |
| CN103797010B (zh) | 2011-06-20 | 2016-02-24 | 因塞特控股公司 | 作为jak抑制剂的氮杂环丁烷基苯基、吡啶基或吡嗪基甲酰胺衍生物 |
| TW201313721A (zh) | 2011-08-18 | 2013-04-01 | Incyte Corp | 作為jak抑制劑之環己基氮雜環丁烷衍生物 |
| UA111854C2 (uk) | 2011-09-07 | 2016-06-24 | Інсайт Холдінгс Корпорейшн | Способи і проміжні сполуки для отримання інгібіторів jak |
| JP2012012411A (ja) * | 2011-10-03 | 2012-01-19 | Ssp Co Ltd | 経口投与用製剤 |
| EP2797600A4 (en) | 2011-12-28 | 2015-09-16 | Pozen Inc | IMPROVED COMPOSITIONS AND METHODS OF DISTRIBUTING OMEPRAZOLE AND ACETYL SALICYLIC ACID |
| US9993422B2 (en) | 2012-04-18 | 2018-06-12 | SpecGx LLC | Immediate release, abuse deterrent pharmaceutical compositions |
| TW201406761A (zh) | 2012-05-18 | 2014-02-16 | Incyte Corp | 做爲jak抑制劑之哌啶基環丁基取代之吡咯并吡啶及吡咯并嘧啶衍生物 |
| US9855286B2 (en) | 2012-05-18 | 2018-01-02 | Gruenenthal Gmbh | Pharmaceutical composition comprising (1r,4r)-6′-fluoro-N,N-di methyl-4-phenyl-4′,9′-dihydro-3′H-spiro[cyclohexane-1,1′-pyrano-[3,4,b]indol]-4-amine and a salicylic acid component |
| US9308196B2 (en) * | 2012-05-18 | 2016-04-12 | Gruenenthal Gmbh | Pharmaceutical composition comprising (1 r,4r) -6'-fluoro-N ,N-dimethyl-4-phenyl-4',9'-d ihydro-3'H-spiro[cyclohexane-1,1'-pyrano-[3,4,b]indol]-4-amine and an oxicam |
| US20130310435A1 (en) | 2012-05-18 | 2013-11-21 | Gruenenthal Gmbh | Pharmaceutical Composition Comprising (1r,4r)-6'-fluoro-N, N-dimethyl-4-phenyl-4,9' -dihydro-3'H-spiro[cyclohexane-1,1' -pyrano[3,4,b]indol]-4-amine and Paracetamol or Propacetamol |
| US20130310385A1 (en) | 2012-05-18 | 2013-11-21 | Gruenenthal Gmbh | Pharmaceutical Composition Comprising (1r,4r)-6'-fluoro-N,N-dimethyl-4-phenyl-4',9'-dihydro-3'H-spiro[cyclohexane-1,1'-pyrano[3,4,b]indol]-4-amine and Antidepressants |
| US9320729B2 (en) | 2012-05-18 | 2016-04-26 | Gruenenthal Gmbh | Pharmaceutical composition comprising (1r,4r)-6′-flouro-N,N-dimethyl-4-phenyl-4′,9′-dihydro-3′H-spiro[cyclohexane-1,1′-pyrano-[3,4,b]indol]-4-amine and a propionic acid derivative |
| PH12020551186B1 (en) | 2012-11-15 | 2024-03-20 | Incyte Holdings Corp | Sustained-release dosage forms of ruxolitinib |
| RS62867B1 (sr) | 2013-03-06 | 2022-02-28 | Incyte Holdings Corp | Postupci i intermedijeri za dobijanje inhibitora jak |
| CA2901802C (en) | 2013-03-15 | 2021-03-02 | Mallinckrodt Llc | Abuse deterrent solid dosage form for immediate release with functional score |
| JP2013216701A (ja) * | 2013-07-29 | 2013-10-24 | Ssp Co Ltd | 経口投与用製剤 |
| WO2015016256A1 (ja) * | 2013-07-30 | 2015-02-05 | ライオン株式会社 | 錠剤 |
| SMT202000315T1 (it) | 2013-08-07 | 2020-07-08 | Incyte Corp | Forme di dosaggio a rilascio prolungato per un inibitore di jak1 |
| US9498467B2 (en) | 2014-05-30 | 2016-11-22 | Incyte Corporation | Treatment of chronic neutrophilic leukemia (CNL) and atypical chronic myeloid leukemia (aCML) by inhibitors of JAK1 |
| WO2016004170A1 (en) | 2014-07-03 | 2016-01-07 | Mallinckrodt Llc | Abuse deterrent immediate release formulations comprising non-cellulose polysaccharides |
| JP6983161B2 (ja) | 2015-09-15 | 2021-12-17 | プラクシス・バイオリサーチ・エルエルシー | フェンカンファミンのプロドラッグ |
| WO2018197932A1 (en) | 2017-04-27 | 2018-11-01 | Dr. Reddy's Laboratories Ltd. | Pharmaceutical compositions of ketorolac |
| WO2019113487A1 (en) | 2017-12-08 | 2019-06-13 | Incyte Corporation | Low dose combination therapy for treatment of myeloproliferative neoplasms |
| SG11202007164UA (en) | 2018-01-30 | 2020-08-28 | Incyte Corp | Processes for preparing (1 -(3-fluoro-2-(trifluoromethyl)isonicotinyl)piperidine-4-one) |
| SMT202400306T1 (it) | 2018-03-30 | 2024-09-16 | Incyte Corp | Trattamento dell'idrosadenite suppurativa utilizzando inibitori di jak. |
| JP7170437B2 (ja) * | 2018-06-29 | 2022-11-14 | 小林製薬株式会社 | 内服用医薬組成物 |
| EP3856160A4 (en) | 2018-09-25 | 2022-07-06 | SpecGx LLC | ABUSE-PROOF IMMEDIATE RELEASE CAPSULE DOSAGE FORMS |
| US11779541B2 (en) * | 2019-03-26 | 2023-10-10 | Johnson & Johnson Consumer Inc. | Immediate release dosage form |
| JP7717065B2 (ja) | 2019-11-22 | 2025-08-01 | インサイト コーポレーション | Alk2阻害剤及びjak2阻害剤を含む併用療法 |
| JP7499025B2 (ja) * | 2019-12-27 | 2024-06-13 | 小林製薬株式会社 | 内服用医薬組成物 |
| US11833155B2 (en) | 2020-06-03 | 2023-12-05 | Incyte Corporation | Combination therapy for treatment of myeloproliferative neoplasms |
| US11324727B2 (en) | 2020-07-15 | 2022-05-10 | Schabar Research Associates, Llc | Unit oral dose compositions composed of naproxen sodium and famotidine for the treatment of acute pain and the reduction of the severity of heartburn and/or the risk of heartburn |
| US12514846B2 (en) | 2020-07-15 | 2026-01-06 | Schabar Research Associates Llc | Unit oral dose compositions composed of ibuprofen or a pharmaceutically acceptable salt thereof and famotidine or a pharmaceutically acceptable salt thereof for the treatment of acute pain and the reduction of the severity and/or risk of heartburn and/or upset stomach |
| KR20230051164A (ko) | 2020-07-15 | 2023-04-17 | 샤바르 리서치 어소시에이츠 엘엘씨 | 급성 통증의 치료 및 속쓰림의 중증도 및/또는 위험의 감소를 위한 이부프로펜 및 파모티딘으로 구성된 단위 경구 투여 조성물 |
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| CA2061520C (en) * | 1991-03-27 | 2003-04-22 | Lawrence J. Daher | Delivery system for enhanced onset and increased potency |
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| ZA959469B (en) | 1994-11-15 | 1996-05-15 | South African Druggists Ltd | Pharmaceutical composition |
-
1999
- 1999-09-10 DE DE69905380T patent/DE69905380T2/de not_active Expired - Lifetime
- 1999-09-10 WO PCT/DK1999/000480 patent/WO2000015195A1/en not_active Ceased
- 1999-09-10 EP EP99941418A patent/EP1109534B1/en not_active Expired - Lifetime
- 1999-09-10 PT PT99941418T patent/PT1109534E/pt unknown
- 1999-09-10 US US09/786,864 patent/US6713089B1/en not_active Expired - Lifetime
- 1999-09-10 TR TR2001/00708T patent/TR200100708T2/xx unknown
- 1999-09-10 EA EA200100331A patent/EA004032B1/ru not_active IP Right Cessation
- 1999-09-10 AU AU55045/99A patent/AU5504599A/en not_active Abandoned
- 1999-09-10 CA CA002343148A patent/CA2343148C/en not_active Expired - Lifetime
- 1999-09-10 JP JP2000569779A patent/JP5026635B2/ja not_active Expired - Lifetime
- 1999-09-10 DK DK99941418T patent/DK1109534T3/da active
- 1999-09-10 AT AT99941418T patent/ATE232382T1/de active
- 1999-09-10 ES ES99941418T patent/ES2190241T3/es not_active Expired - Lifetime
-
2011
- 2011-10-14 JP JP2011227314A patent/JP5622703B2/ja not_active Expired - Lifetime
Also Published As
| Publication number | Publication date |
|---|---|
| AU5504599A (en) | 2000-04-03 |
| CA2343148A1 (en) | 2000-03-23 |
| PT1109534E (pt) | 2003-06-30 |
| US6713089B1 (en) | 2004-03-30 |
| DK1109534T3 (da) | 2003-06-10 |
| ATE232382T1 (de) | 2003-02-15 |
| EP1109534B1 (en) | 2003-02-12 |
| JP2002524492A (ja) | 2002-08-06 |
| JP2012082197A (ja) | 2012-04-26 |
| DE69905380D1 (de) | 2003-03-20 |
| DE69905380T2 (de) | 2003-11-27 |
| EP1109534A1 (en) | 2001-06-27 |
| JP5622703B2 (ja) | 2014-11-12 |
| EA200100331A1 (ru) | 2001-08-27 |
| WO2000015195A1 (en) | 2000-03-23 |
| EA004032B1 (ru) | 2003-12-25 |
| TR200100708T2 (tr) | 2001-07-23 |
| JP5026635B2 (ja) | 2012-09-12 |
| CA2343148C (en) | 2005-11-15 |
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