|
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
|
|
JP2527107B2
(ja)
†
|
1991-04-16 |
1996-08-21 |
日本新薬株式会社 |
固体分散体の製造方法
|
|
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
|
|
EP0665010B1
(en)
*
|
1992-10-16 |
2002-09-11 |
Nippon Shinyaku Company, Limited |
Method of manufacturing wax matrices
|
|
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
|
|
US20020006438A1
(en)
*
|
1998-09-25 |
2002-01-17 |
Benjamin Oshlack |
Sustained release hydromorphone formulations exhibiting bimodal characteristics
|
|
US5965161A
(en)
*
|
1994-11-04 |
1999-10-12 |
Euro-Celtique, S.A. |
Extruded multi-particulates
|
|
DE19629753A1
(de)
*
|
1996-07-23 |
1998-01-29 |
Basf Ag |
Verfahren zur Herstellung von festen Arzneiformen
|
|
TW474824B
(en)
|
1996-09-13 |
2002-02-01 |
Basf Ag |
The production of 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
|
|
ES2412409T3
(es)
|
1997-12-22 |
2013-07-11 |
Euro-Celtique S.A. |
Forma farmacéutica para dosificación oral que comprende una combinación de un agonista opiáceo y un antagonista opiáceo
|
|
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
|
|
WO2001032148A1
(en)
|
1999-10-29 |
2001-05-10 |
Euro-Celtique, S.A. |
Controlled release hydrocodone formulations
|
|
US7364752B1
(en)
|
1999-11-12 |
2008-04-29 |
Abbott Laboratories |
Solid dispersion pharamaceutical formulations
|
|
CA2359945C
(en)
*
|
1999-11-12 |
2011-04-26 |
Abbott Laboratories |
Inhibitors of crystallization in a solid dispersion
|
|
DE19960494A1
(de)
*
|
1999-12-15 |
2001-06-21 |
Knoll Ag |
Vorrichtung und Verfahren zum Herstellen von festen wirkstoffhaltigen Formen
|
|
IL151058A0
(en)
|
2000-02-08 |
2003-04-10 |
Euro Celtique Sa |
Controlled-release compositions containing opioid agonist and antagonist
|
|
SI1299104T1
(sl)
|
2000-02-08 |
2009-10-31 |
Euro Celtique Sa |
Oralne formulacije opioidnih agonistov, varne pred zlorabo
|
|
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
|
|
CN101317825A
(zh)
|
2000-10-30 |
2008-12-10 |
欧罗赛铁克股份有限公司 |
控释氢可酮制剂
|
|
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
|
|
US20030044458A1
(en)
|
2001-08-06 |
2003-03-06 |
Curtis Wright |
Oral dosage form comprising a therapeutic agent and an adverse-effect agent
|
|
US7914818B2
(en)
|
2001-08-06 |
2011-03-29 |
Purdue Pharma L.P. |
Opioid agonist formulations with releasable and sequestered antagonist
|
|
WO2003013433A2
(en)
|
2001-08-06 |
2003-02-20 |
Euro-Celtique S.A. |
Sequestered antagonist formulations
|
|
ES2320748T5
(es)
*
|
2002-04-05 |
2017-02-20 |
Euro-Celtique S.A. |
Matriz para la liberación sostenida, invariable e independiente de compuestos activos
|
|
US7776314B2
(en)
|
2002-06-17 |
2010-08-17 |
Grunenthal Gmbh |
Abuse-proofed dosage system
|
|
EP2422773A3
(en)
|
2002-09-20 |
2012-04-18 |
Alpharma, Inc. |
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
|
|
EP1572190B1
(en)
*
|
2002-12-17 |
2007-04-18 |
Abbott GmbH & Co. KG |
Formulation comprising fenofibric acid, a physiologically acceptable salt or derivative thereof
|
|
US20080051411A1
(en)
*
|
2002-12-17 |
2008-02-28 |
Cink Russell D |
Salts of Fenofibric Acid and Pharmaceutical Formulations 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
|
|
AU2004232370B2
(en)
|
2003-04-21 |
2009-12-10 |
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
|
|
US8075872B2
(en)
|
2003-08-06 |
2011-12-13 |
Gruenenthal Gmbh |
Abuse-proofed dosage form
|
|
US20070048228A1
(en)
|
2003-08-06 |
2007-03-01 |
Elisabeth Arkenau-Maric |
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
|
|
DE102004032051A1
(de)
|
2004-07-01 |
2006-01-19 |
Grünenthal GmbH |
Verfahren zur Herstellung einer gegen Missbrauch gesicherten, festen Darreichungsform
|
|
DE10361596A1
(de)
|
2003-12-24 |
2005-09-29 |
Grünenthal GmbH |
Verfahren zur Herstellung einer gegen Missbrauch gesicherten Darreichungsform
|
|
US8377952B2
(en)
|
2003-08-28 |
2013-02-19 |
Abbott Laboratories |
Solid pharmaceutical dosage formulation
|
|
US8025899B2
(en)
|
2003-08-28 |
2011-09-27 |
Abbott Laboratories |
Solid pharmaceutical dosage form
|
|
EP1663229B1
(en)
|
2003-09-25 |
2010-04-14 |
Euro-Celtique S.A. |
Pharmaceutical combinations of hydrocodone and naltrexone
|
|
WO2005053652A1
(en)
|
2003-12-04 |
2005-06-16 |
Pfizer Products Inc. |
Multiparticulate crystalline drug compositions containing a poloxamer and a glyceride
|
|
BRPI0416535A
(pt)
*
|
2003-12-04 |
2007-01-09 |
Pfizer Prod Inc |
processo de congelamento por vaporização empregando um extrusor para preparar composições de azitromicina de multiparticulado contendo preferivelmente um poloxámero e um glicerìdeo
|
|
EP1691786A1
(en)
*
|
2003-12-04 |
2006-08-23 |
Pfizer Products Inc. |
Multiparticulate compositions with improved stability
|
|
WO2005053639A2
(en)
*
|
2003-12-04 |
2005-06-16 |
Pfizer Products Inc. |
Controlled release multiparticulates formed with dissolution enhancers
|
|
US6984403B2
(en)
*
|
2003-12-04 |
2006-01-10 |
Pfizer Inc. |
Azithromycin dosage forms with reduced side effects
|
|
ATE399536T1
(de)
*
|
2003-12-04 |
2008-07-15 |
Pfizer Prod Inc |
Verfahren zur herstellung von pharmazeutischen multiteilchenförmigen produkten
|
|
EP1689368B1
(en)
*
|
2003-12-04 |
2016-09-28 |
Bend Research, Inc |
Spray-congeal process using an extruder for preparing multiparticulate crystalline drug compositions
|
|
AU2004294818A1
(en)
*
|
2003-12-04 |
2005-06-16 |
Pfizer Products Inc. |
Azithromycin multiparticulate dosage forms by liquid-based processes
|
|
CA2548834C
(en)
*
|
2003-12-09 |
2009-08-11 |
Euro-Celtique S.A. |
Tamper resistant co-extruded dosage form containing an active agent and an adverse agent and process of making same
|
|
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
|
|
EP2343073A3
(en)
|
2003-12-11 |
2011-10-12 |
Sepracor Inc. |
Combination of a sedative and a neurotransmitter modulator, and methods for improving sleep quality and treating depression
|
|
TW201509943A
(zh)
*
|
2004-03-30 |
2015-03-16 |
Euro Celtique Sa |
含有小於25ppm14-羥可待因酮之羥可酮鹽酸鹽之組成物、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
|
|
DK1748762T3
(en)
*
|
2004-05-28 |
2014-03-17 |
Abbvie Deutschland |
Dosage form which can be obtained from a powder mixture comprising an inorganic pigment
|
|
EP1604666A1
(en)
|
2004-06-08 |
2005-12-14 |
Euro-Celtique S.A. |
Opioids for the treatment of the Chronic Obstructive Pulmonary Disease (COPD)
|
|
EP1604667A1
(en)
|
2004-06-08 |
2005-12-14 |
Euro-Celtique S.A. |
Opioids for the treatment of the restless leg syndrome
|
|
CA2916869A1
(en)
|
2004-06-12 |
2005-12-29 |
Jane C. Hirsh |
Abuse-deterrent drug formulations
|
|
DE102004032049A1
(de)
|
2004-07-01 |
2006-01-19 |
Grünenthal GmbH |
Gegen Missbrauch gesicherte, orale Darreichungsform
|
|
EP1771160A2
(en)
*
|
2005-01-28 |
2007-04-11 |
Euroceltique S.A. |
Alcohol resistant dosage forms
|
|
DE102005005449A1
(de)
|
2005-02-04 |
2006-08-10 |
Grünenthal GmbH |
Verfahren zur Herstellung einer gegen Missbrauch gesicherten Darreichungsform
|
|
EP1695700A1
(en)
*
|
2005-02-28 |
2006-08-30 |
Euro-Celtique S.A. |
Dosage form containing oxycodone and naloxone
|
|
EP1702558A1
(en)
|
2005-02-28 |
2006-09-20 |
Euro-Celtique S.A. |
Method and device for the assessment of bowel function
|
|
CA2612864A1
(en)
*
|
2005-07-05 |
2007-01-11 |
Abbott Gmbh & Co. Kg |
Composition and dosage form comprising a solid or semi-solid matrix
|
|
ES2571032T3
(es)
|
2005-08-08 |
2016-05-23 |
Abbvie Deutschland |
Composiciones de itraconazol con biodisponibilidad mejorada
|
|
DK1912626T3
(en)
*
|
2005-08-08 |
2016-08-01 |
Abbvie Deutschland |
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
|
|
ES2636657T3
(es)
|
2006-06-19 |
2017-10-06 |
Alpharma Pharmaceuticals Llc |
Composición farmacéutica
|
|
EP2112925A4
(en)
*
|
2006-11-15 |
2013-01-09 |
Abbott Lab |
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
|
|
EP2067471B1
(en)
|
2007-12-06 |
2018-02-14 |
Durect Corporation |
Oral pharmaceutical dosage forms
|
|
US8623418B2
(en)
|
2007-12-17 |
2014-01-07 |
Alpharma Pharmaceuticals Llc |
Pharmaceutical composition
|
|
US8383152B2
(en)
|
2008-01-25 |
2013-02-26 |
Gruenenthal Gmbh |
Pharmaceutical dosage form
|
|
TWI524904B
(zh)
|
2008-05-09 |
2016-03-11 |
歌林達股份有限公司 |
製備醫藥用固體劑型,尤指錠劑之方法,及製備固體劑型,尤指錠劑之前驅物之方法
|
|
CA2737400C
(en)
*
|
2008-10-07 |
2016-11-22 |
Astrazeneca Uk Limited |
Pharmaceutical formulation 514
|
|
US20100260844A1
(en)
|
2008-11-03 |
2010-10-14 |
Scicinski Jan J |
Oral pharmaceutical dosage forms
|
|
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
|
|
UY32487A
(es)
|
2009-03-10 |
2010-06-30 |
Euro Celtique Sa |
Composiciones farmacéuticas de liberación inmediata comprendiendo oxicodona y naloxona
|
|
NZ596668A
(en)
|
2009-07-22 |
2013-09-27 |
Gruenenthal Chemie |
Oxidation-stabilized tamper-resistant dosage form
|
|
JP5667183B2
(ja)
|
2009-07-22 |
2015-02-12 |
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 |
加熱溶融押出成型した制御放出性投与剤型
|
|
CN102573755A
(zh)
*
|
2009-09-18 |
2012-07-11 |
巴斯夫欧洲公司 |
制备具有低水溶性的物质的制剂的方法
|
|
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
|
|
MX2013002293A
(es)
|
2010-09-02 |
2013-05-09 |
Gruenenthal Gmbh |
Forma de dosificacion resistente a alteracion que comprende un polimero anionico.
|
|
ES2486791T3
(es)
|
2010-09-02 |
2014-08-19 |
Grünenthal GmbH |
Forma de dosificación resistente a la manipulación que comprende una sal inorgánica
|
|
KR101572336B1
(ko)
|
2010-12-22 |
2015-11-26 |
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
|
|
PE20141650A1
(es)
|
2011-07-29 |
2014-11-22 |
Gruenenthal Chemie |
Tableta a prueba de alteracion que proporciona liberacion inmediata del farmaco
|
|
EA201400172A1
(ru)
|
2011-07-29 |
2014-06-30 |
Грюненталь Гмбх |
Устойчивая к разрушению таблетка, которая обеспечивает немедленное высвобождение лекарственного средства
|
|
WO2013127831A1
(en)
|
2012-02-28 |
2013-09-06 |
Grünenthal GmbH |
Tamper-resistant dosage form comprising pharmacologically active compound and anionic polymer
|
|
ES2692944T3
(es)
|
2012-04-18 |
2018-12-05 |
Grünenthal GmbH |
Forma de dosificación farmacéutica resistente a la manipulación y resistente a la descarga rápida de la dosis
|
|
US10064945B2
(en)
|
2012-05-11 |
2018-09-04 |
Gruenenthal Gmbh |
Thermoformed, tamper-resistant pharmaceutical dosage form containing zinc
|
|
TWI643859B
(zh)
|
2012-07-16 |
2018-12-11 |
羅德科技公司 |
改良之類鴉片合成方法
|
|
CN104507947B
(zh)
|
2012-07-16 |
2017-06-27 |
罗德科技公司 |
用于改进的阿片样物质合成的方法
|
|
WO2014123899A1
(en)
|
2013-02-05 |
2014-08-14 |
Purdue Pharma L.P. |
Tamper resistant pharmaceutical formulations
|
|
CA2905131A1
(en)
|
2013-03-15 |
2014-09-18 |
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
|
|
BR112015026549A2
(pt)
|
2013-05-29 |
2017-07-25 |
Gruenenthal Gmbh |
forma de dosagem à prova de violação contendo uma ou mais partículas
|
|
US9737490B2
(en)
|
2013-05-29 |
2017-08-22 |
Grünenthal GmbH |
Tamper resistant dosage form with bimodal release profile
|
|
AU2014289187B2
(en)
|
2013-07-12 |
2019-07-11 |
Grunenthal Gmbh |
Tamper-resistant dosage form containing ethylene-vinyl acetate polymer
|
|
UA116567C2
(uk)
|
2013-07-23 |
2018-04-10 |
Євро-Селтік С.А. |
Комбінація оксикодону та налоксону для застосування в лікуванні болю у пацієнтів, які страждають від болю та захворювання, що призводить до дисбактеріозу кишечнику та/або підвищує ризик кишкової бактеріальної транслокації
|
|
CA2919602C
(en)
|
2013-08-02 |
2018-03-13 |
Johnson Matthey Public Limited Company |
Process for the preparation of oxymorphone
|
|
AU2014356581C1
(en)
|
2013-11-26 |
2020-05-28 |
Grunenthal Gmbh |
Preparation of a powdery pharmaceutical composition by means of cryo-milling
|
|
US9938285B2
(en)
|
2014-01-15 |
2018-04-10 |
Rhodes Technologies |
Process for improved oxymorphone synthesis
|
|
EP3094634A1
(en)
|
2014-01-15 |
2016-11-23 |
Rhodes Technologies |
Process for improved oxycodone synthesis
|
|
US9062063B1
(en)
|
2014-03-21 |
2015-06-23 |
Johnson Matthey Public Limited Company |
Forms of oxymorphone hydrochloride
|
|
MX2016014738A
(es)
|
2014-05-12 |
2017-03-06 |
Gruenenthal Gmbh |
Formulacion en capsula de liberacion inmediata resistente a alteraciones que comprende tapentadol.
|
|
CN106456550A
(zh)
|
2014-05-26 |
2017-02-22 |
格吕伦塔尔有限公司 |
避免乙醇剂量倾泻的多颗粒
|
|
US9918979B2
(en)
|
2015-01-29 |
2018-03-20 |
Johnson Matthey Public Limited Company |
Process of preparing low ABUK oxymorphone hydrochloride
|
|
BR112017021475A2
(pt)
|
2015-04-24 |
2018-07-10 |
Gruenenthal Gmbh |
forma de dosagem resistente à adulteração (tamper) com liberação imediata e resistência contra extração de solvente
|
|
CA2998259A1
(en)
|
2015-09-10 |
2017-03-16 |
Grunenthal 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
|
|
JP7258561B2
(ja)
|
2016-07-06 |
2023-04-17 |
オリエント ファーマ シーオー.,エルティーディー. |
薬物組成物、バリヤー層及び薬物層を有している経口投与形態
|