|
DE4031881C2
(de)
*
|
1990-10-08 |
1994-02-24 |
Sanol Arznei Schwarz Gmbh |
Lösungsmittelfreie, oral zu verabreichende pharmazeutische Zubereitung mit verzögerter Wirkstoffreisetzung und Verfahren zu deren Herstellung
|
|
ATE159426T1
(de)
†
|
1991-04-16 |
1997-11-15 |
Nippon Shinyaku Co Ltd |
Verfahren zur herstellung einer festen dispersion
|
|
ATE147261T1
(de)
*
|
1992-01-13 |
1997-01-15 |
Pfizer |
Verfahren zur herstellung von tabletten mit hoher festigkeit
|
|
JPH0656659A
(ja)
*
|
1992-06-10 |
1994-03-01 |
Natl Sci Council |
直接打錠できる薬学組成物及びその錠剤の製造法
|
|
KR100291362B1
(ko)
*
|
1992-10-16 |
2001-09-17 |
니뽄 신야쿠 가부시키가이샤 |
왁스매트릭스의제법
|
|
IL110139A0
(en)
*
|
1993-06-28 |
1994-10-07 |
Howard Foundation |
Pharmaceutically-active antioxidants
|
|
GB9422154D0
(en)
*
|
1994-11-03 |
1994-12-21 |
Euro Celtique Sa |
Pharmaceutical compositions and method of producing the same
|
|
US5965161A
(en)
|
1994-11-04 |
1999-10-12 |
Euro-Celtique, S.A. |
Extruded multi-particulates
|
|
US20020006438A1
(en)
*
|
1998-09-25 |
2002-01-17 |
Benjamin Oshlack |
Sustained release hydromorphone formulations exhibiting bimodal characteristics
|
|
DE19629753A1
(de)
|
1996-07-23 |
1998-01-29 |
Basf Ag |
Verfahren zur Herstellung von festen Arzneiformen
|
|
HRP970485A2
(en)
|
1996-09-13 |
1998-08-31 |
Joerg Rosenberg |
Process for producing solid pharmaceutical forms
|
|
DE19710213A1
(de)
*
|
1997-03-12 |
1998-09-17 |
Basf Ag |
Verfahren zur Herstellung von festen Kombinationsarzneiformen
|
|
DE19753298A1
(de)
|
1997-12-01 |
1999-06-02 |
Basf Ag |
Verfahren zur Herstellung von festen Dosierungsformen
|
|
NZ505193A
(en)
|
1997-12-22 |
2003-03-28 |
Euro Celtique S |
Opioid agonist/antagonist combinations
|
|
US6375957B1
(en)
*
|
1997-12-22 |
2002-04-23 |
Euro-Celtique, S.A. |
Opioid agonist/opioid antagonist/acetaminophen combinations
|
|
DE19812688A1
(de)
|
1998-03-23 |
1999-09-30 |
Basf Ag |
Verfahren zur Herstellung von festen Dosierungsformen
|
|
DE19840256A1
(de)
|
1998-09-03 |
2000-03-09 |
Basf Ag |
Verfahren zur Herstellung von beschichteten festen Dosierungsformen
|
|
DE19841244A1
(de)
|
1998-09-09 |
2000-03-16 |
Knoll Ag |
Verfahren und Vorrichtung zum Herstellen von Tabletten
|
|
DE19843904A1
(de)
|
1998-09-24 |
2000-03-30 |
Basf Ag |
Feste Dosierungsform mit polymerem Bindemittel
|
|
DE19847618A1
(de)
|
1998-10-15 |
2000-04-20 |
Basf Ag |
Verfahren zur Herstellung von festen Dosierungsformen
|
|
DE19901383A1
(de)
|
1999-01-15 |
2000-07-20 |
Knoll Ag |
Verfahren zur Herstellung unterschiedlicher fester Dosierungsformen
|
|
DE19918325A1
(de)
|
1999-04-22 |
2000-10-26 |
Euro Celtique Sa |
Verfahren zur Herstellung von Arzneiformen mit regulierter Wirkstofffreisetzung mittels Extrusion
|
|
CA2389235C
(en)
|
1999-10-29 |
2007-07-17 |
Euro-Celtique, S.A. |
Controlled release hydrocodone formulations
|
|
US7364752B1
(en)
|
1999-11-12 |
2008-04-29 |
Abbott Laboratories |
Solid dispersion pharamaceutical formulations
|
|
JP5767429B2
(ja)
*
|
1999-11-12 |
2015-08-19 |
アッヴィ・インコーポレイテッド |
固体分散剤中の結晶化阻害剤
|
|
DE19960494A1
(de)
*
|
1999-12-15 |
2001-06-21 |
Knoll Ag |
Vorrichtung und Verfahren zum Herstellen von festen wirkstoffhaltigen Formen
|
|
BR0108379A
(pt)
|
2000-02-08 |
2002-11-05 |
Euro Celtique Sa |
Composições de liberação controlada contendo agonista e antagonista opióide, método para a preparação de uma formulação em dosagem de analgésico opióide de liberação controlada com potência analgésica aumentada e sistema de administração através da derme para um analgésico opióide
|
|
ES2312413T3
(es)
|
2000-02-08 |
2009-03-01 |
Euro-Celtique S.A. |
Composiciones de liberacion controlada que contienen un agonista y antagonista de opioide.
|
|
DE10017102A1
(de)
|
2000-04-06 |
2001-10-11 |
Basf Ag |
Verfahren zur Herstellung von festen Kreatin-Dosierungsformen und dadurch erhältliche Dosierungsformen
|
|
DE10026698A1
(de)
*
|
2000-05-30 |
2001-12-06 |
Basf Ag |
Selbstemulgierende Wirkstoffformulierung und Verwendung dieser Formulierung
|
|
KR100968128B1
(ko)
|
2000-10-30 |
2010-07-06 |
유로-셀티크 소시에떼 아노뉨 |
서방성 하이드로코돈 제형
|
|
UA81224C2
(uk)
|
2001-05-02 |
2007-12-25 |
Euro Celtic S A |
Дозована форма оксикодону та її застосування
|
|
US20030065002A1
(en)
|
2001-05-11 |
2003-04-03 |
Endo Pharmaceuticals, Inc. |
Abuse-resistant controlled-release opioid dosage form
|
|
US20030068375A1
(en)
|
2001-08-06 |
2003-04-10 |
Curtis Wright |
Pharmaceutical formulation containing gelling agent
|
|
CA2457361C
(en)
|
2001-08-06 |
2008-11-04 |
Christopher Breder |
Opioid agonist formulations with releasable and sequestered antagonist
|
|
US20030044458A1
(en)
|
2001-08-06 |
2003-03-06 |
Curtis Wright |
Oral dosage form comprising a therapeutic agent and an adverse-effect agent
|
|
AU2002324624A1
(en)
|
2001-08-06 |
2003-02-24 |
Euro-Celtique S.A. |
Sequestered antagonist formulations
|
|
JP4755810B2
(ja)
|
2002-04-05 |
2011-08-24 |
ユーロ−セルティーク エス.エイ. |
オキシコドン及びナロキソンを含有する医薬製剤
|
|
US7776314B2
(en)
|
2002-06-17 |
2010-08-17 |
Grunenthal Gmbh |
Abuse-proofed dosage system
|
|
AU2003270778B2
(en)
|
2002-09-20 |
2009-10-08 |
Alpharma Pharmaceuticals, Llc |
Sequestering subunit and related compositions and methods
|
|
DE10247037A1
(de)
*
|
2002-10-09 |
2004-04-22 |
Abbott Gmbh & Co. Kg |
Herstellung von festen Dosierungsformen unter Verwendung eines vernetzten nichtthermoplastischen Trägers
|
|
SI1575569T1
(sl)
|
2002-12-13 |
2010-12-31 |
Durect Corp |
Oralni sistem dostave zdravila, ki obsega visokoviskozne tekoče nosilne materiale
|
|
US20080051411A1
(en)
*
|
2002-12-17 |
2008-02-28 |
Cink Russell D |
Salts of Fenofibric Acid and Pharmaceutical Formulations Thereof
|
|
WO2004054568A1
(en)
*
|
2002-12-17 |
2004-07-01 |
Abbott Gmbh & Co. Kg |
Formulation comprising fenofibric acid, a physiologically acceptable salt or derivative thereof
|
|
JP2006518380A
(ja)
*
|
2003-01-31 |
2006-08-10 |
スミスクライン・ビーチャム・コーポレイション |
固体分散体組成物
|
|
WO2004093819A2
(en)
|
2003-04-21 |
2004-11-04 |
Euro-Celtique, S.A. |
Tamper resistant dosage form comprising co-extruded, adverse agent particles and process of making same
|
|
MY135852A
(en)
|
2003-04-21 |
2008-07-31 |
Euro Celtique Sa |
Pharmaceutical products
|
|
DE10361596A1
(de)
|
2003-12-24 |
2005-09-29 |
Grünenthal GmbH |
Verfahren zur Herstellung einer gegen Missbrauch gesicherten Darreichungsform
|
|
DE102004032051A1
(de)
|
2004-07-01 |
2006-01-19 |
Grünenthal GmbH |
Verfahren zur Herstellung einer gegen Missbrauch gesicherten, festen Darreichungsform
|
|
US20070048228A1
(en)
|
2003-08-06 |
2007-03-01 |
Elisabeth Arkenau-Maric |
Abuse-proofed dosage form
|
|
US8075872B2
(en)
*
|
2003-08-06 |
2011-12-13 |
Gruenenthal Gmbh |
Abuse-proofed dosage form
|
|
DE102005005446A1
(de)
*
|
2005-02-04 |
2006-08-10 |
Grünenthal GmbH |
Bruchfeste Darreichungsformen mit retardierter Freisetzung
|
|
DE10336400A1
(de)
|
2003-08-06 |
2005-03-24 |
Grünenthal GmbH |
Gegen Missbrauch gesicherte Darreichungsform
|
|
US8025899B2
(en)
|
2003-08-28 |
2011-09-27 |
Abbott Laboratories |
Solid pharmaceutical dosage form
|
|
US8377952B2
(en)
|
2003-08-28 |
2013-02-19 |
Abbott Laboratories |
Solid pharmaceutical dosage formulation
|
|
EP1663229B1
(en)
|
2003-09-25 |
2010-04-14 |
Euro-Celtique S.A. |
Pharmaceutical combinations of hydrocodone and naltrexone
|
|
WO2005053651A1
(en)
*
|
2003-12-04 |
2005-06-16 |
Pfizer Products Inc. |
Multiparticulate compositions with improved stability
|
|
CA2549225A1
(en)
*
|
2003-12-04 |
2005-06-16 |
Pfizer Products Inc. |
Spray-congeal process using an extruder for preparing multiparticulate crystalline drug compositions containing preferably a poloxamer and a glyceride
|
|
KR20060109481A
(ko)
*
|
2003-12-04 |
2006-10-20 |
화이자 프로덕츠 인코포레이티드 |
바람직하게는 폴록사머와 글리세라이드를 함유하는다미립자 아지트로마이신 조성물의 제조를 위해 압출기를사용하는 분무응결 방법
|
|
DK1691787T3
(da)
*
|
2003-12-04 |
2008-09-22 |
Pfizer Prod Inc |
Fremgangsmåde til at danne småpartikler
|
|
WO2005053639A2
(en)
*
|
2003-12-04 |
2005-06-16 |
Pfizer Products Inc. |
Controlled release multiparticulates formed with dissolution enhancers
|
|
WO2005053652A1
(en)
|
2003-12-04 |
2005-06-16 |
Pfizer Products Inc. |
Multiparticulate crystalline drug compositions containing a poloxamer and a glyceride
|
|
US6984403B2
(en)
*
|
2003-12-04 |
2006-01-10 |
Pfizer Inc. |
Azithromycin dosage forms with reduced side effects
|
|
KR20060092281A
(ko)
*
|
2003-12-04 |
2006-08-22 |
화이자 프로덕츠 인크. |
액체 기초 방법에 의한 아지트로마이신 복합입자 투여형
|
|
US8883204B2
(en)
|
2003-12-09 |
2014-11-11 |
Purdue Pharma L.P. |
Tamper resistant co-extruded dosage form containing an active agent and an adverse agent and process of making same
|
|
EP1691892B1
(en)
*
|
2003-12-09 |
2007-02-28 |
Euro-Celtique S.A. |
Tamper resistant co-extruded dosage form containing an active agent and an adverse agent and process of making same
|
|
JP5646126B2
(ja)
|
2003-12-11 |
2014-12-24 |
サノビオン ファーマシューティカルズ インクSunovion Pharmaceuticals Inc. |
鎮静剤と神経伝達物質調節剤の併用、および睡眠の質の向上方法および鬱の治療方法
|
|
TWI483944B
(zh)
|
2004-03-30 |
2015-05-11 |
Euro Celtique Sa |
含有小於25ppm14-羥可待因酮之羥可酮鹽酸鹽組成物、醫藥劑型、延遲釋出口服劑型及醫藥上可以接受的包裝
|
|
RS50817B
(sr)
*
|
2004-03-30 |
2010-08-31 |
Euro-Celtique S.A. |
Dozni oblik otporan na promene koji sadrži adsorbenti i sredstvo sa suprotnim dejstvom
|
|
EP1748762B1
(de)
*
|
2004-05-28 |
2013-12-18 |
AbbVie Deutschland GmbH & Co KG |
Dosierungsform, erhältlich aus einer ein anorganisches pigment umfassenden pulvermischung
|
|
EP1604667A1
(en)
|
2004-06-08 |
2005-12-14 |
Euro-Celtique S.A. |
Opioids for the treatment of the restless leg syndrome
|
|
EP1604666A1
(en)
|
2004-06-08 |
2005-12-14 |
Euro-Celtique S.A. |
Opioids for the treatment of the Chronic Obstructive Pulmonary Disease (COPD)
|
|
LT1765292T
(lt)
|
2004-06-12 |
2018-01-10 |
Collegium Pharmaceutical, Inc. |
Nuo piktnaudžiavimo apsaugotos vaistų formos
|
|
DE102004032049A1
(de)
|
2004-07-01 |
2006-01-19 |
Grünenthal GmbH |
Gegen Missbrauch gesicherte, orale Darreichungsform
|
|
CN101132772B
(zh)
*
|
2005-01-28 |
2012-05-09 |
欧洲凯尔特公司 |
耐醇剂型
|
|
DE102005005449A1
(de)
|
2005-02-04 |
2006-08-10 |
Grünenthal GmbH |
Verfahren zur Herstellung einer gegen Missbrauch gesicherten Darreichungsform
|
|
EP1702558A1
(en)
|
2005-02-28 |
2006-09-20 |
Euro-Celtique S.A. |
Method and device for the assessment of bowel function
|
|
EP1695700A1
(en)
*
|
2005-02-28 |
2006-08-30 |
Euro-Celtique S.A. |
Dosage form containing oxycodone and naloxone
|
|
CA2612864A1
(en)
*
|
2005-07-05 |
2007-01-11 |
Abbott Gmbh & Co. Kg |
Composition and dosage form comprising a solid or semi-solid matrix
|
|
US8486456B2
(en)
|
2005-08-08 |
2013-07-16 |
Abbott Gmbh & Co., Kg |
Itraconazole compositions with improved bioavailability
|
|
WO2007017249A1
(en)
*
|
2005-08-08 |
2007-02-15 |
Abbott Gmbh & Co. Kg |
Dosage forms with improved bioavailability
|
|
EP1813276A1
(en)
*
|
2006-01-27 |
2007-08-01 |
Euro-Celtique S.A. |
Tamper resistant dosage forms
|
|
EP1832281A1
(en)
|
2006-03-10 |
2007-09-12 |
Abbott GmbH & Co. KG |
Process for producing a solid dispersion of an active ingredient
|
|
AU2007261451A1
(en)
|
2006-06-19 |
2007-12-27 |
Alpharma Pharmaceuticals, Llc |
Pharmaceutical compositions
|
|
WO2008067164A2
(en)
*
|
2006-11-15 |
2008-06-05 |
Abbott Laboratories |
Solid pharmaceutical dosage formulations
|
|
GB0624880D0
(en)
*
|
2006-12-14 |
2007-01-24 |
Johnson Matthey Plc |
Improved method for making analgesics
|
|
DE102007011485A1
(de)
|
2007-03-07 |
2008-09-11 |
Grünenthal GmbH |
Darreichungsform mit erschwertem Missbrauch
|
|
US8415401B2
(en)
|
2007-12-06 |
2013-04-09 |
Durect Corporation |
Oral pharmaceutical dosage forms
|
|
US8623418B2
(en)
|
2007-12-17 |
2014-01-07 |
Alpharma Pharmaceuticals Llc |
Pharmaceutical composition
|
|
WO2009092601A1
(en)
|
2008-01-25 |
2009-07-30 |
Grünenthal GmbH |
Pharmaceutical dosage form
|
|
HRP20161307T1
(hr)
|
2008-05-09 |
2016-12-02 |
Grünenthal GmbH |
Postupak za pripravu praškaste formulacije međuproizvoda i konačni kruti oblik doziranja uz korištenje koraka zgrušavanja raspršivanjem
|
|
CN102238945B
(zh)
*
|
2008-10-07 |
2014-10-29 |
阿斯利康(英国)有限公司 |
药物制剂514
|
|
US20100260844A1
(en)
|
2008-11-03 |
2010-10-14 |
Scicinski Jan J |
Oral pharmaceutical dosage forms
|
|
WO2010099508A1
(en)
|
2009-02-26 |
2010-09-02 |
Theraquest Biosciences, Inc. |
Extended release oral pharmaceutical compositions of 3-hydroxy-n-methylmorphinan and method of use
|
|
KR20140141727A
(ko)
|
2009-03-10 |
2014-12-10 |
유로-셀티큐 에스.에이. |
옥시코돈 및 날록손을 포함하는 즉시 방출 제약 조성물
|
|
ES2428938T3
(es)
|
2009-07-22 |
2013-11-12 |
Grünenthal GmbH |
Forma de dosificación resistente a la manipulación y estabilizada frente a la oxidación
|
|
ES2534908T3
(es)
|
2009-07-22 |
2015-04-30 |
Grünenthal GmbH |
Forma de dosificación de liberación controlada extruida por fusión en caliente
|
|
JP2013505210A
(ja)
*
|
2009-09-18 |
2013-02-14 |
ビーエーエスエフ ソシエタス・ヨーロピア |
水への溶解性が低い物質の製剤を製造する方法
|
|
US10668060B2
(en)
|
2009-12-10 |
2020-06-02 |
Collegium Pharmaceutical, Inc. |
Tamper-resistant pharmaceutical compositions of opioids and other drugs
|
|
EP2531176B1
(en)
|
2010-02-03 |
2016-09-07 |
Grünenthal GmbH |
Preparation of a powdery pharmaceutical composition by means of an extruder
|
|
AU2011297892B2
(en)
|
2010-09-02 |
2014-05-29 |
Grunenthal Gmbh |
Tamper resistant dosage form comprising an anionic polymer
|
|
AU2011297901B2
(en)
|
2010-09-02 |
2014-07-31 |
Grunenthal Gmbh |
Tamper resistant dosage form comprising inorganic salt
|
|
KR101647267B1
(ko)
|
2010-12-22 |
2016-08-09 |
퍼듀 퍼머 엘피 |
케이싱된 탬퍼 저항성 제어 방출 투여 형태
|
|
PH12013501345A1
(en)
|
2010-12-23 |
2022-10-24 |
Purdue Pharma Lp |
Tamper resistant solid oral dosage forms
|
|
RS56528B1
(sr)
|
2011-07-29 |
2018-02-28 |
Gruenenthal Gmbh |
Tableta za trenutno oslobađanje leka rezistentna na zloupotrebu
|
|
AU2012292418B2
(en)
|
2011-07-29 |
2017-02-16 |
Grunenthal Gmbh |
Tamper-resistant tablet providing immediate drug release
|
|
EP2819656A1
(en)
|
2012-02-28 |
2015-01-07 |
Grünenthal GmbH |
Tamper-resistant dosage form comprising pharmacologically active compound and anionic polymer
|
|
EP2838512B1
(en)
|
2012-04-18 |
2018-08-22 |
Grünenthal GmbH |
Tamper resistant and dose-dumping resistant pharmaceutical dosage form
|
|
US10064945B2
(en)
|
2012-05-11 |
2018-09-04 |
Gruenenthal Gmbh |
Thermoformed, tamper-resistant pharmaceutical dosage form containing zinc
|
|
JP6236446B2
(ja)
|
2012-07-16 |
2017-11-22 |
ローズ テクノロジーズ |
改善されたオピオイド合成方法
|
|
TWI643860B
(zh)
|
2012-07-16 |
2018-12-11 |
羅德科技公司 |
改良之類鴉片合成方法
|
|
PE20151301A1
(es)
|
2013-02-05 |
2015-09-16 |
Purdue Pharma Lp |
Formulaciones farmaceuticas resistentes a la manipulacion indebida
|
|
US9555113B2
(en)
|
2013-03-15 |
2017-01-31 |
Durect Corporation |
Compositions with a rheological modifier to reduce dissolution variability
|
|
US10751287B2
(en)
|
2013-03-15 |
2020-08-25 |
Purdue Pharma L.P. |
Tamper resistant pharmaceutical formulations
|
|
AU2014273227B2
(en)
|
2013-05-29 |
2019-08-15 |
Grunenthal Gmbh |
Tamper-resistant dosage form containing one or more particles
|
|
BR112015029616A2
(pt)
|
2013-05-29 |
2017-07-25 |
Gruenenthal Gmbh |
forma de dosagem resistente à adulteração com perfil de liberação bimodal
|
|
CA2917136C
(en)
|
2013-07-12 |
2022-05-31 |
Grunenthal Gmbh |
Tamper-resistant dosage form containing ethylene-vinyl acetate polymer
|
|
US10071089B2
(en)
|
2013-07-23 |
2018-09-11 |
Euro-Celtique S.A. |
Combination of oxycodone and naloxone for use in treating pain in patients suffering from pain and a disease resulting in intestinal dysbiosis and/or increasing the risk for intestinal bacterial translocation
|
|
WO2015015146A1
(en)
|
2013-08-02 |
2015-02-05 |
Johnson Matthey Public Limited Company |
Process for the preparation of oxymorphone
|
|
BR112016010482B1
(pt)
|
2013-11-26 |
2022-11-16 |
Grünenthal GmbH |
Preparação de uma composição farmacêutica em pó por meio de criomoagem
|
|
US9938285B2
(en)
|
2014-01-15 |
2018-04-10 |
Rhodes Technologies |
Process for improved oxymorphone synthesis
|
|
CN106029670A
(zh)
|
2014-01-15 |
2016-10-12 |
罗德科技公司 |
改进的羟考酮合成的方法
|
|
US9062063B1
(en)
|
2014-03-21 |
2015-06-23 |
Johnson Matthey Public Limited Company |
Forms of oxymorphone hydrochloride
|
|
JP2017518980A
(ja)
|
2014-05-12 |
2017-07-13 |
グリュネンタール・ゲゼルシャフト・ミト・ベシュレンクテル・ハフツング |
タペンタドールを含む、改変防止即時放出カプセル製剤
|
|
CA2949422A1
(en)
|
2014-05-26 |
2015-12-03 |
Grunenthal Gmbh |
Multiparticles safeguarded against ethanolic dose-dumping
|
|
US9918979B2
(en)
|
2015-01-29 |
2018-03-20 |
Johnson Matthey Public Limited Company |
Process of preparing low ABUK oxymorphone hydrochloride
|
|
MX2017013637A
(es)
|
2015-04-24 |
2018-03-08 |
Gruenenthal Gmbh |
Forma de dosificacion resistente a alteraciones con liberacion inmediata y resistencia contra la extraccion por solventes.
|
|
WO2017042325A1
(en)
|
2015-09-10 |
2017-03-16 |
Grünenthal GmbH |
Protecting oral overdose with abuse deterrent immediate release formulations
|
|
US9737530B1
(en)
|
2016-06-23 |
2017-08-22 |
Collegium Pharmaceutical, Inc. |
Process of making stable abuse-deterrent oral formulations
|
|
CA3028450A1
(en)
|
2016-07-06 |
2018-01-11 |
Durect Corporation |
Oral dosage form with drug composition, barrier layer and drug layer
|