TW299236B - - Google Patents
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- TW299236B TW299236B TW081108615A TW81108615A TW299236B TW 299236 B TW299236 B TW 299236B TW 081108615 A TW081108615 A TW 081108615A TW 81108615 A TW81108615 A TW 81108615A TW 299236 B TW299236 B TW 299236B
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- methyl
- release
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- polymer
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Classifications
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- A—HUMAN NECESSITIES
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
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- A61K9/28—Dragees; Coated pills or tablets, e.g. with film or compression coating
- A61K9/2806—Coating materials
- A61K9/2833—Organic macromolecular compounds
- A61K9/286—Polysaccharides, e.g. gums; Cyclodextrin
- A61K9/2866—Cellulose; Cellulose derivatives, e.g. hydroxypropyl methylcellulose
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- A—HUMAN NECESSITIES
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- A61K9/20—Pills, tablets, discs, rods
- A61K9/2072—Pills, tablets, discs, rods characterised by shape, structure or size; Tablets with holes, special break lines or identification marks; Partially coated tablets; Disintegrating flat shaped forms
- A61K9/2086—Layered tablets, e.g. bilayer tablets; Tablets of the type inert core-active coat
- A61K9/209—Layered tablets, e.g. bilayer tablets; Tablets of the type inert core-active coat containing drug in at least two layers or in the core and in at least one outer layer
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- 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
- A61K9/28—Dragees; Coated pills or tablets, e.g. with film or compression coating
- A61K9/2806—Coating materials
- A61K9/2813—Inorganic compounds
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- 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
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- 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
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- General Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Epidemiology (AREA)
- General Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Inorganic Chemistry (AREA)
- Chemical Kinetics & Catalysis (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)
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| Application Number | Priority Date | Filing Date | Title |
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| GB919123044A GB9123044D0 (en) | 1991-10-30 | 1991-10-30 | Compositions |
| GB919123026A GB9123026D0 (en) | 1991-10-30 | 1991-10-30 | Compositions |
| GB929203364A GB9203364D0 (en) | 1992-02-18 | 1992-02-18 | Compositions |
Publications (1)
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| TW299236B true TW299236B (https=) | 1997-03-01 |
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| TW081108615A TW299236B (https=) | 1991-10-30 | 1992-10-29 |
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| EP (1) | EP0546593B1 (https=) |
| JP (1) | JPH05194188A (https=) |
| KR (1) | KR930007439A (https=) |
| AU (1) | AU666880B2 (https=) |
| BE (1) | BE1005490A3 (https=) |
| CA (1) | CA2081709C (https=) |
| CH (1) | CH685536A5 (https=) |
| CZ (1) | CZ325792A3 (https=) |
| DE (1) | DE69222006T2 (https=) |
| ES (1) | ES2106818T3 (https=) |
| FR (1) | FR2683146B1 (https=) |
| GB (1) | GB2262445B (https=) |
| IE (1) | IE922775A1 (https=) |
| IL (1) | IL103593A0 (https=) |
| IT (1) | IT1263253B (https=) |
| LU (1) | LU88186A1 (https=) |
| MX (1) | MX9206236A (https=) |
| NO (1) | NO924183L (https=) |
| NZ (1) | NZ244921A (https=) |
| TW (1) | TW299236B (https=) |
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| US5609884A (en) * | 1992-08-31 | 1997-03-11 | G. D. Searle & Co. | Controlled release naproxen sodium plus naproxen combination tablet |
| GB9401894D0 (en) | 1994-02-01 | 1994-03-30 | Rhone Poulenc Rorer Ltd | New compositions of matter |
| JPH07223970A (ja) * | 1994-02-10 | 1995-08-22 | Tanabe Seiyaku Co Ltd | 消化管内適所放出製剤 |
| US6887461B1 (en) * | 1998-10-26 | 2005-05-03 | Genetics Institute, Llc | Method of using IL-11 for treating mucositis |
| US6548084B2 (en) | 1995-07-20 | 2003-04-15 | Smithkline Beecham Plc | Controlled release compositions |
| JPH0940561A (ja) * | 1995-08-02 | 1997-02-10 | Fujitsukusu Kk | 瀉下剤 |
| US5837284A (en) * | 1995-12-04 | 1998-11-17 | Mehta; Atul M. | Delivery of multiple doses of medications |
| US5922736A (en) * | 1995-12-04 | 1999-07-13 | Celegene Corporation | Chronic, bolus administration of D-threo methylphenidate |
| US6486177B2 (en) * | 1995-12-04 | 2002-11-26 | Celgene Corporation | Methods for treatment of cognitive and menopausal disorders with D-threo methylphenidate |
| US5800834A (en) * | 1996-06-10 | 1998-09-01 | Spireas; Spiridon | Liquisolid systems and methods of preparing same |
| US8022095B2 (en) * | 1996-08-16 | 2011-09-20 | Pozen, Inc. | Methods of treating headaches using 5-HT agonists in combination with long-acting NSAIDs |
| GB9706089D0 (en) * | 1997-03-24 | 1997-05-14 | Scherer Ltd R P | Pharmaceutical composition |
| US6962997B1 (en) * | 1997-05-22 | 2005-11-08 | Celgene Corporation | Process and intermediates for resolving piperidyl acetamide steroisomers |
| IN186245B (https=) | 1997-09-19 | 2001-07-14 | Ranbaxy Lab Ltd | |
| US6607751B1 (en) * | 1997-10-10 | 2003-08-19 | Intellipharamaceutics Corp. | Controlled release delivery device for pharmaceutical agents incorporating microbial polysaccharide gum |
| AU2004222771B2 (en) * | 1998-07-30 | 2006-09-21 | Pfizer Inc. | Prevention of Migraine Recurrence |
| GB9816556D0 (en) * | 1998-07-30 | 1998-09-30 | Pfizer Ltd | Therapy |
| US6602521B1 (en) * | 1998-09-29 | 2003-08-05 | Impax Pharmaceuticals, Inc. | Multiplex drug delivery system suitable for oral administration |
| US20080118556A1 (en) * | 1998-11-02 | 2008-05-22 | Elan Corporation, Plc | Modified Release of Compositions Containing a Combination of Carbidopa, Levodopa and Entacapone |
| EP1126826B3 (en) * | 1998-11-02 | 2019-05-15 | Alkermes Pharma Ireland Limited | Multiparticulate modified release composition of methylphenidate |
| US20090149479A1 (en) * | 1998-11-02 | 2009-06-11 | Elan Pharma International Limited | Dosing regimen |
| US20060240105A1 (en) * | 1998-11-02 | 2006-10-26 | Elan Corporation, Plc | Multiparticulate modified release composition |
| PE20001302A1 (es) | 1998-11-27 | 2000-11-30 | Hoffmann La Roche | Preparaciones de una combinacion farmaceutica que contiene carvedilol e hidroclorotiazida |
| US6270807B1 (en) | 1999-03-02 | 2001-08-07 | L. Perrigo Company | Taste-masked pharmaceutical composition |
| US6632451B2 (en) * | 1999-06-04 | 2003-10-14 | Dexcel Pharma Technologies Ltd. | Delayed total release two pulse gastrointestinal drug delivery system |
| US20040258750A1 (en) * | 1999-06-28 | 2004-12-23 | Gerard Alaux | Timed dual release dosage forms comprising a short acting hypnotic or a salt thereof |
| EP1064938A1 (en) * | 1999-06-28 | 2001-01-03 | Sanofi-Synthelabo | Pharmaceutical dosage forms for controlled release producing at least a timed pulse |
| US20020028240A1 (en) * | 2000-04-17 | 2002-03-07 | Toyohiro Sawada | Timed-release compression-coated solid composition for oral administration |
| US6620431B1 (en) | 2000-04-17 | 2003-09-16 | Charles Signorino | Shellac film coatings providing release at selected pH and method |
| IT1318571B1 (it) * | 2000-06-09 | 2003-08-27 | Farmaka Srl | Composizioni cosmetiche per la cura del cuoio capelluto e dei capelli. |
| US6500457B1 (en) | 2000-08-14 | 2002-12-31 | Peirce Management, Llc | Oral pharmaceutical dosage forms for pulsatile delivery of an antiarrhythmic agent |
| WO2002066002A2 (en) * | 2001-02-14 | 2002-08-29 | Glaxo Wellcome S.A. | Pharmaceutical formulation |
| AU4061702A (en) * | 2001-05-15 | 2003-04-03 | Mcneil-Ppc, Inc. | Dip coating compositions containing starch or dextrin |
| US20030070584A1 (en) * | 2001-05-15 | 2003-04-17 | Cynthia Gulian | Dip coating compositions containing cellulose ethers |
| US20030072731A1 (en) * | 2001-05-15 | 2003-04-17 | Cynthia Gulian | Dip coating compositions containing starch or dextrin |
| US8309118B2 (en) * | 2001-09-28 | 2012-11-13 | Mcneil-Ppc, Inc. | Film forming compositions containing sucralose |
| US20030091630A1 (en) * | 2001-10-25 | 2003-05-15 | Jenny Louie-Helm | Formulation of an erodible, gastric retentive oral dosage form using in vitro disintegration test data |
| US20030104052A1 (en) * | 2001-10-25 | 2003-06-05 | Bret Berner | Gastric retentive oral dosage form with restricted drug release in the lower gastrointestinal tract |
| CA2409552A1 (en) | 2001-10-25 | 2003-04-25 | Depomed, Inc. | Gastric retentive oral dosage form with restricted drug release in the lower gastrointestinal tract |
| CA2470495A1 (en) * | 2001-12-24 | 2003-07-17 | Teva Pharmaceutical Industries Ltd. | Dosage form with a core tablet of active ingredient sheathed in a compressed annular body of powder or granular material, and process and tooling for producing it |
| US20040052843A1 (en) * | 2001-12-24 | 2004-03-18 | Lerner E. Itzhak | Controlled release dosage forms |
| CA2480403A1 (en) * | 2002-04-08 | 2003-10-23 | Lavipharm Laboratories Inc. | Drug-complex microparticles and methods of making/using same |
| AU2003249478A1 (en) * | 2002-07-19 | 2004-02-09 | Ranbaxy Laboratories Limited | Taste masked sumatriptan tablets and processes for their preparation |
| US7429619B2 (en) * | 2002-08-02 | 2008-09-30 | Mcneil Consumer Healthcare | Polyacrylic film forming compositions |
| US20040068000A1 (en) * | 2002-10-02 | 2004-04-08 | Mintong Guo | Compression coated tablets |
| US20080220074A1 (en) * | 2002-10-04 | 2008-09-11 | Elan Corporation Plc | Gamma radiation sterilized nanoparticulate docetaxel compositions and methods of making same |
| MY148805A (en) | 2002-10-16 | 2013-05-31 | Takeda Pharmaceutical | Controlled release preparation |
| WO2004060355A1 (en) * | 2002-12-26 | 2004-07-22 | Pozen Inc. | Multilayer Dosage Forms Containing NSAIDs and Triptans |
| EP1607092A4 (en) * | 2003-03-17 | 2010-12-15 | Takeda Pharmaceutical | COMPOSITIONS WITH CONTROLLED RELEASE |
| US20040241252A1 (en) * | 2003-05-29 | 2004-12-02 | Abney Christopher Charles | Pharmaceutical compositions for oral administration comprising lithium carbonate, processes of making the same, and methods of administering the same |
| JP2006527195A (ja) * | 2003-06-06 | 2006-11-30 | グラクソ グループ リミテッド | トリプタンおよびnsaidを含む組成物 |
| US7390503B1 (en) * | 2003-08-22 | 2008-06-24 | Barr Laboratories, Inc. | Ondansetron orally disintegrating tablets |
| WO2005030179A1 (en) * | 2003-09-29 | 2005-04-07 | Cj Corporation | Sustained-release formulations |
| GB0400452D0 (en) * | 2004-01-09 | 2004-02-11 | Norton Healthcare Ltd | A pharmaceutical composition |
| GB0403628D0 (en) * | 2004-02-18 | 2004-03-24 | Arrow Group Ltd | Compression-coated tablets and the manufacture thereof |
| US20050239830A1 (en) * | 2004-04-26 | 2005-10-27 | Vikram Khetani | Methods of diminishing co-abuse potential |
| EP1750677B1 (en) * | 2004-05-28 | 2017-02-01 | Imaginot Pty Ltd. | Oral therapeutic compound delivery system |
| US8216610B2 (en) * | 2004-05-28 | 2012-07-10 | Imaginot Pty Ltd. | Oral paracetamol formulations |
| US20060024361A1 (en) * | 2004-07-28 | 2006-02-02 | Isa Odidi | Disintegrant assisted controlled release technology |
| KR20070043806A (ko) * | 2004-07-29 | 2007-04-25 | 사노피-아벤티스 | pH에 매우 의존적인 용해도를 가지는 활성 성분의 제어방출을 위한 약제학적 다층 정제 |
| US20060024368A1 (en) * | 2004-07-30 | 2006-02-02 | Reza Fassihi | Compressed composite delivery system for release-rate modulation of bioactives |
| US10624858B2 (en) * | 2004-08-23 | 2020-04-21 | Intellipharmaceutics Corp | Controlled release composition using transition coating, and method of preparing same |
| WO2006035313A1 (en) * | 2004-09-29 | 2006-04-06 | Aurobindo Pharma Ltd | Solid unit dosage forms of 5-ht1 agonist |
| US20060240043A1 (en) * | 2004-10-08 | 2006-10-26 | Meyerson Laurence R | Methods and compositions for treating migraine pain |
| US20060121112A1 (en) * | 2004-12-08 | 2006-06-08 | Elan Corporation, Plc | Topiramate pharmaceutical composition |
| CA2591247A1 (en) * | 2004-12-09 | 2006-06-15 | Celgene Corporation | Treatment of patients suffering from a disease having a family history or diagnosis of tics or tourette's syndrome with d-threo methylphenidate |
| AU2006235483B2 (en) * | 2005-04-12 | 2010-11-25 | Elan Pharma International Limited | Controlled release compositions comprising a cephalosporin for the treatment of a bacterial infection |
| WO2007037790A2 (en) * | 2005-06-08 | 2007-04-05 | Elan Corporation, Plc | Modified release famciclovir compositions |
| US9757455B2 (en) * | 2005-11-28 | 2017-09-12 | Johnson & Johnson Consumer Inc. | Oral therapeutic compound delivery system |
| US10064828B1 (en) | 2005-12-23 | 2018-09-04 | Intellipharmaceutics Corp. | Pulsed extended-pulsed and extended-pulsed pulsed drug delivery systems |
| US9265732B2 (en) | 2006-03-06 | 2016-02-23 | Pozen Inc. | Dosage forms for administering combinations of drugs |
| EP1993518A4 (en) * | 2006-03-06 | 2012-12-12 | Pozen Inc | DOSAGE FORMS FOR THE ADMINISTRATION OF MEDICINAL COMBINATIONS |
| US20190083399A9 (en) * | 2006-04-03 | 2019-03-21 | Isa Odidi | Drug delivery composition |
| CA2648280C (en) | 2006-04-03 | 2014-03-11 | Isa Odidi | Controlled release delivery device comprising an organosol coat |
| US10960077B2 (en) * | 2006-05-12 | 2021-03-30 | Intellipharmaceutics Corp. | Abuse and alcohol resistant drug composition |
| UA96457C2 (ru) | 2006-08-03 | 2011-11-10 | Нитек Фарма Аг | Лечение ревматоидного артрита глюкокортикоидами с отсроченным высвобождением |
| EP2124556B1 (en) | 2006-10-09 | 2014-09-03 | Charleston Laboratories, Inc. | Pharmaceutical compositions |
| KR100885029B1 (ko) * | 2007-02-07 | 2009-02-23 | 지엘팜텍 주식회사 | 경구투여용 서방성 삼중정제 |
| EP1970056A1 (en) * | 2007-03-15 | 2008-09-17 | Polichem S.A. | Time-specific delayed/pulsatile release dosage forms |
| US9138430B2 (en) * | 2007-12-27 | 2015-09-22 | Mylan Specialty L.P. | Formulation and method for the release of paroxetine in the large intestine |
| ES2620672T3 (es) | 2008-01-09 | 2017-06-29 | Charleston Laboratories, Inc. | Comprimidos de doble capa que comprenden oxicodona y prometazina |
| AU2009241847B2 (en) * | 2008-04-28 | 2014-07-10 | Zogenix, Inc. | Novel formulations for treatment of migraine |
| AU2010207740B2 (en) * | 2009-01-26 | 2016-06-16 | Nitec Pharma Ag | Delayed-release glucocorticoid treatment of asthma |
| NZ582836A (en) * | 2009-01-30 | 2011-06-30 | Nitec Pharma Ag | Delayed-release glucocorticoid treatment of rheumatoid arthritis by improving signs and symptoms, showing major or complete clinical response and by preventing from joint damage |
| WO2010100657A2 (en) * | 2009-03-04 | 2010-09-10 | Fdc Limited | A novel oral controlled release dosage forms for water soluble drugs |
| WO2011006012A1 (en) | 2009-07-08 | 2011-01-13 | Charleston Laboratories Inc. | Pharmaceutical compositions |
| GB201003734D0 (en) | 2010-03-05 | 2010-04-21 | Univ Strathclyde | Delayed prolonged drug delivery |
| GB201003731D0 (en) * | 2010-03-05 | 2010-04-21 | Univ Strathclyde | Immediate/delayed drug delivery |
| GB201003766D0 (en) | 2010-03-05 | 2010-04-21 | Univ Strathclyde | Pulsatile drug release |
| HUE034955T2 (en) | 2010-12-22 | 2018-03-28 | Purdue Pharma Lp | Encased tamper resistant controlled release dosage forms |
| PH12013501345A1 (en) | 2010-12-23 | 2022-10-24 | Purdue Pharma Lp | Tamper resistant solid oral dosage forms |
| MX2015010041A (es) | 2013-02-05 | 2015-10-30 | Purdue Pharma Lp | Formulacion farmaceuticas resistentes a la alteracion. |
| EP2963013A4 (en) * | 2013-02-27 | 2016-09-14 | Shionogi & Co | INDOLE AND AZAINDOLE DERIVATIVES HAVING AMPK ACTIVATION ACTIVITY EACH |
| US10751287B2 (en) | 2013-03-15 | 2020-08-25 | Purdue Pharma L.P. | Tamper resistant pharmaceutical formulations |
| BR112016029127A2 (pt) * | 2014-06-13 | 2017-08-22 | Avery Dennison Corp | adesivos sensíveis à pressão melhorados usados para aplicações médicas |
| JP2019507181A (ja) | 2016-03-04 | 2019-03-14 | チャールストン ラボラトリーズ,インコーポレイテッド | 医薬組成物 |
Family Cites Families (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4892742A (en) * | 1985-11-18 | 1990-01-09 | Hoffmann-La Roche Inc. | Controlled release compositions with zero order release |
| DE3720757A1 (de) * | 1987-06-24 | 1989-01-05 | Bayer Ag | Dhp-manteltablette |
| DE3814532A1 (de) * | 1988-04-29 | 1989-11-09 | Bayer Ag | Dhp-retard-zubereitung |
| US4880636A (en) * | 1988-05-13 | 1989-11-14 | Franz Robert M | Film coated tablet of ranitidine HCl |
| US5032406A (en) * | 1989-02-21 | 1991-07-16 | Norwich Eaton Pharmaceuticals, Inc. | Dual-action tablet |
| US5085865A (en) * | 1989-04-12 | 1992-02-04 | Warner-Lambert Company | Sustained release pharmaceutical preparations containing an analgesic and a decongestant |
| GB9104890D0 (en) * | 1991-03-08 | 1991-04-24 | Glaxo Group Ltd | Compositions |
-
1992
- 1992-10-23 DE DE69222006T patent/DE69222006T2/de not_active Expired - Lifetime
- 1992-10-23 ES ES92203262T patent/ES2106818T3/es not_active Expired - Lifetime
- 1992-10-23 EP EP92203262A patent/EP0546593B1/en not_active Expired - Lifetime
- 1992-10-28 GB GB9222662A patent/GB2262445B/en not_active Expired - Lifetime
- 1992-10-29 IL IL103593A patent/IL103593A0/xx unknown
- 1992-10-29 CA CA002081709A patent/CA2081709C/en not_active Expired - Lifetime
- 1992-10-29 NZ NZ244921A patent/NZ244921A/en unknown
- 1992-10-29 NO NO92924183A patent/NO924183L/no unknown
- 1992-10-29 KR KR1019920020034A patent/KR930007439A/ko not_active Withdrawn
- 1992-10-29 FR FR9212932A patent/FR2683146B1/fr not_active Expired - Lifetime
- 1992-10-29 MX MX9206236A patent/MX9206236A/es unknown
- 1992-10-29 LU LU88186A patent/LU88186A1/fr unknown
- 1992-10-29 AU AU27469/92A patent/AU666880B2/en not_active Ceased
- 1992-10-29 BE BE9200937A patent/BE1005490A3/fr not_active IP Right Cessation
- 1992-10-29 IE IE277592A patent/IE922775A1/en not_active IP Right Cessation
- 1992-10-29 CZ CS923257A patent/CZ325792A3/cs unknown
- 1992-10-29 CH CH3390/92A patent/CH685536A5/fr not_active IP Right Cessation
- 1992-10-29 IT ITRM920788A patent/IT1263253B/it active IP Right Grant
- 1992-10-29 JP JP4291571A patent/JPH05194188A/ja active Pending
- 1992-10-29 TW TW081108615A patent/TW299236B/zh active
-
1994
- 1994-05-31 US US08/250,948 patent/US5425950A/en not_active Expired - Lifetime
Also Published As
| Publication number | Publication date |
|---|---|
| IT1263253B (it) | 1996-08-05 |
| MX9206236A (es) | 1993-04-01 |
| GB2262445A (en) | 1993-06-23 |
| EP0546593B1 (en) | 1997-09-03 |
| NZ244921A (en) | 1995-04-27 |
| DE69222006D1 (de) | 1997-10-09 |
| ITRM920788A0 (it) | 1992-10-29 |
| CA2081709A1 (en) | 1993-05-01 |
| FR2683146A1 (fr) | 1993-05-07 |
| NO924183D0 (no) | 1992-10-29 |
| CZ325792A3 (en) | 1993-10-13 |
| GB9222662D0 (en) | 1992-12-09 |
| EP0546593A1 (en) | 1993-06-16 |
| KR930007439A (ko) | 1993-05-20 |
| DE69222006T2 (de) | 1998-01-22 |
| ITRM920788A1 (it) | 1994-04-29 |
| LU88186A1 (fr) | 1993-05-17 |
| JPH05194188A (ja) | 1993-08-03 |
| IE922775A1 (en) | 1993-05-05 |
| BE1005490A3 (fr) | 1993-08-10 |
| FR2683146B1 (fr) | 1995-05-12 |
| ES2106818T3 (es) | 1997-11-16 |
| CA2081709C (en) | 2003-09-02 |
| IL103593A0 (en) | 1993-03-15 |
| CH685536A5 (fr) | 1995-08-15 |
| AU666880B2 (en) | 1996-02-29 |
| GB2262445B (en) | 1996-05-15 |
| AU2746992A (en) | 1993-05-06 |
| US5425950A (en) | 1995-06-20 |
| NO924183L (no) | 1993-05-03 |
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