ES2733051T1 - Matriz para liberación sostenida, invariable e independiente de compuestos activos - Google Patents
Matriz para liberación sostenida, invariable e independiente de compuestos activos Download PDFInfo
- Publication number
- ES2733051T1 ES2733051T1 ES17154462T ES17154462T ES2733051T1 ES 2733051 T1 ES2733051 T1 ES 2733051T1 ES 17154462 T ES17154462 T ES 17154462T ES 17154462 T ES17154462 T ES 17154462T ES 2733051 T1 ES2733051 T1 ES 2733051T1
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- ES
- Spain
- Prior art keywords
- pharmaceutically acceptable
- acceptable salt
- pharmaceutical formulation
- naloxone
- formulation according
- 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.)
- Pending
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- 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
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/47—Quinolines; Isoquinolines
- A61K31/485—Morphinan derivatives, e.g. morphine, codeine
-
- 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
- A61K9/0012—Galenical forms characterised by the site of application
- A61K9/0053—Mouth and digestive tract, i.e. intraoral and peroral administration
-
- 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
-
- 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
- A61K9/1617—Organic compounds, e.g. phospholipids, fats
-
- 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
- A61K9/20—Pills, tablets, discs, rods
-
- 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
- A61K9/20—Pills, tablets, discs, rods
- A61K9/2004—Excipients; Inactive ingredients
- A61K9/2013—Organic compounds, e.g. phospholipids, fats
-
- 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
- A61K9/2013—Organic compounds, e.g. phospholipids, fats
- A61K9/2018—Sugars, or sugar alcohols, e.g. lactose, mannitol; Derivatives thereof, e.g. polysorbates
-
- 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
- A61K9/2022—Organic macromolecular compounds
- A61K9/205—Polysaccharides, e.g. alginate, gums; Cyclodextrin
- A61K9/2054—Cellulose; Cellulose derivatives, e.g. hydroxypropyl methylcellulose
-
- 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
- A61K9/2072—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
- A61K9/2077—Tablets comprising drug-containing microparticles in a substantial amount of supporting matrix; Multiparticulate tablets
-
- 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
- A61K9/2095—Tabletting processes; Dosage units made by direct compression of powders or specially processed granules, by eliminating solvents, by melt-extrusion, by injection molding, by 3D printing
-
- 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
- A61K9/2833—Organic macromolecular compounds
- A61K9/286—Polysaccharides, e.g. gums; Cyclodextrin
- A61K9/2866—Cellulose; Cellulose derivatives, e.g. hydroxypropyl methylcellulose
-
- 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
-
- 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
- A61K9/70—Web, sheet or filament bases ; Films; Fibres of the matrix type containing drug
-
- 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
-
- 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
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
- A61P1/10—Laxatives
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P13/00—Drugs for disorders of the urinary system
- A61P13/12—Drugs for disorders of the urinary system of the kidneys
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P17/00—Drugs for dermatological disorders
- A61P17/04—Antipruritics
-
- 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
-
- 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
- A61P25/30—Drugs for disorders of the nervous system for treating abuse or dependence
- A61P25/36—Opioid-abuse
-
- 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
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- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Chemical & Material Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Pharmacology & Pharmacy (AREA)
- Animal Behavior & Ethology (AREA)
- Epidemiology (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Organic Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Biophysics (AREA)
- Molecular Biology (AREA)
- Emergency Medicine (AREA)
- Biomedical Technology (AREA)
- Neurosurgery (AREA)
- Neurology (AREA)
- Addiction (AREA)
- Pain & Pain Management (AREA)
- Nutrition Science (AREA)
- Inorganic Chemistry (AREA)
- Physiology (AREA)
- Dermatology (AREA)
- Urology & Nephrology (AREA)
- Rheumatology (AREA)
- Psychiatry (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Medicinal Preparation (AREA)
- Medical Treatment And Welfare Office Work (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
Abstract
Una formulación farmacéutica que comprende una matriz, en la que dicha matriz comprende oxicodona o una sal farmacéuticamente aceptable de la misma, naloxona o una sal farmacéuticamente aceptable de la misma, y etilcelulosa o un alcohol graso.
Claims (15)
1. Una formulación farmacéutica que comprende una matriz, en la que dicha matriz comprende oxicodona o una sal farmacéuticamente aceptable de la misma, naloxona o una sal farmacéuticamente aceptable de la misma, y etilcelulosa o un alcohol graso.
2. La formulación farmacéutica según la reivindicación 1, en la que la etilcelulosa o el alcohol graso está comprendido en la formulación como retardante.
3. La formulación farmacéutica según la reivindicación 1 o 2, en la que dicha matriz comprende oxicodona o una sal farmacéuticamente aceptable de la misma, naloxona o una sal farmacéuticamente aceptable de la misma, etilcelulosa, lactosa, talco y estearato de magnesio.
4. La formulación farmacéutica según la reivindicación 1 o 2, en la que dicha matriz comprende oxicodona o una sal farmacéuticamente aceptable de la misma, naloxona o una sal farmacéuticamente aceptable de la misma, un alcohol graso, celulosa microcristalina, povidona, talco y estearato de magnesio, en el que dicho alcohol graso es preferiblemente alcohol estearilo.
5. La formulación farmacéutica según una cualquiera de las reivindicaciones anteriores, en la que la formulación es una formulación oral.
6. La formulación farmacéutica según una cualquiera de las reivindicaciones anteriores, en la que la formulación es una tableta, tableta multicapa, cápsula o gránulo.
7. La formulación farmacéutica según una cualquiera de las reivindicaciones anteriores, en la que la formulación comprende oxicodona o una sal farmacéuticamente aceptable de la misma en una relación en peso de 15:1, 10:1, 5:1, 4:1, 3:1, 2:1 o 1:1 a naloxona o una sal farmacéuticamente aceptable de la misma.
8. La formulación farmacéutica según una cualquiera de las reivindicaciones 1 a 6, en la que la formulación comprende oxicodona o una sal farmacéuticamente aceptable de la misma en una relación en peso de 2:1 a naloxona o una sal farmacéuticamente aceptable de la misma.
9. La formulación farmacéutica según una cualquiera de las reivindicaciones anteriores, en la que la formulación comprende oxicodona o una sal farmacéuticamente aceptable de la misma en una cantidad de 10 mg y 150 mg.
10. La formulación farmacéutica según una cualquiera de las reivindicaciones anteriores, en la que la formulación comprende naloxona o una sal farmacéuticamente aceptable de la misma en una cantidad de 1 a 50 mg.
11. La formulación farmacéutica según una cualquiera de las reivindicaciones anteriores, en la que la formulación libera 1% a 40% de oxicodona o una sal farmacéuticamente aceptable de la misma y naloxona o una sal farmacéuticamente aceptable de la misma después de 15 minutos, 40% a 85% de oxicodona o un sal farmacéuticamente aceptable de la misma y naloxona o una sal farmacéuticamente aceptable de la misma después de 2 horas, 65% a 100% de oxicodona o una sal farmacéuticamente aceptable de la misma y naloxona o una sal farmacéuticamente aceptable de la misma después de 7 horas y 85% a 100% de oxicodona o un sal farmacéuticamente aceptable de los mismos y naloxona o una sal farmacéuticamente aceptable de los mismos después de 12 horas, según lo determinado por el método de análisis ABC (Basket Method) según USP a pH 1,2 con HPLC.
12. La formulación farmacéutica según una cualquiera de las reivindicaciones anteriores, en la que la formulación comprende oxicodona y naloxona como el hidrocloruro, sulfato, bisulfato, tartrato, nitrato, citrato, bitratrato, fosfato, malato, maleato, bromhidrato, yoduro, fumarato o succinato.
13. La formulación farmacéutica según una cualquiera de las reivindicaciones anteriores, en la que la formulación es estable al almacenamiento.
14. La formulación farmacéutica según una cualquiera de las reivindicaciones anteriores, en la que la matriz es una matriz de difusión.
15. La formulación farmacéutica según una cualquiera de las reivindicaciones anteriores, en la que la formulación es para uso en el tratamiento del dolor y para uso en el tratamiento simultáneo del estreñimiento inducido por opioides.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE10215131A DE10215131A1 (de) | 2002-04-05 | 2002-04-05 | Matrix zur verzögerten, gleichbleibenden und unabhängigen Freisetzung von Wirkstoffen |
DE10215067A DE10215067A1 (de) | 2002-04-05 | 2002-04-05 | Lagerstabiles pharmazeutisches Präparat, das Oxycodon und Naloxon umfasst |
Publications (1)
Publication Number | Publication Date |
---|---|
ES2733051T1 true ES2733051T1 (es) | 2019-11-27 |
Family
ID=28676052
Family Applications (7)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
ES17169621T Pending ES2733044T1 (es) | 2002-04-05 | 2003-04-04 | Composición farmacéutica que contiene oxicodona y naloxona |
ES11177516.9T Expired - Lifetime ES2627298T3 (es) | 2002-04-05 | 2003-04-04 | Preparación farmacéutica que contiene oxicodona y naloxona |
ES11177520.1T Expired - Lifetime ES2608006T3 (es) | 2002-04-05 | 2003-04-04 | Preparación farmacéutica que contiene oxicodona y naloxona |
ES11177518.5T Expired - Lifetime ES2627300T3 (es) | 2002-04-05 | 2003-04-04 | Preparación farmacéutica que contiene oxicodona y naloxona |
ES03720424.5T Expired - Lifetime ES2546010T3 (es) | 2002-04-05 | 2003-04-04 | Preparación farmacéutica que contiene oxicodona y naloxona |
ES03720425.2T Expired - Lifetime ES2320748T5 (es) | 2002-04-05 | 2003-04-04 | Matriz para la liberación sostenida, invariable e independiente de compuestos activos |
ES17154462T Pending ES2733051T1 (es) | 2002-04-05 | 2003-04-04 | Matriz para liberación sostenida, invariable e independiente de compuestos activos |
Family Applications Before (6)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
ES17169621T Pending ES2733044T1 (es) | 2002-04-05 | 2003-04-04 | Composición farmacéutica que contiene oxicodona y naloxona |
ES11177516.9T Expired - Lifetime ES2627298T3 (es) | 2002-04-05 | 2003-04-04 | Preparación farmacéutica que contiene oxicodona y naloxona |
ES11177520.1T Expired - Lifetime ES2608006T3 (es) | 2002-04-05 | 2003-04-04 | Preparación farmacéutica que contiene oxicodona y naloxona |
ES11177518.5T Expired - Lifetime ES2627300T3 (es) | 2002-04-05 | 2003-04-04 | Preparación farmacéutica que contiene oxicodona y naloxona |
ES03720424.5T Expired - Lifetime ES2546010T3 (es) | 2002-04-05 | 2003-04-04 | Preparación farmacéutica que contiene oxicodona y naloxona |
ES03720425.2T Expired - Lifetime ES2320748T5 (es) | 2002-04-05 | 2003-04-04 | Matriz para la liberación sostenida, invariable e independiente de compuestos activos |
Country Status (33)
Country | Link |
---|---|
US (11) | US20050245483A1 (es) |
EP (17) | EP2316429A1 (es) |
JP (5) | JP4620355B2 (es) |
KR (3) | KR20040098050A (es) |
CN (4) | CN1646102B (es) |
AP (2) | AP2043A (es) |
AR (3) | AR039379A1 (es) |
AT (1) | ATE418967T2 (es) |
AU (2) | AU2003224041B2 (es) |
BR (2) | BR0309004A (es) |
CA (3) | CA2478515C (es) |
CO (2) | CO5611100A2 (es) |
CY (5) | CY1108914T1 (es) |
DE (6) | DE20321531U1 (es) |
DK (6) | DK2425824T5 (es) |
ES (7) | ES2733044T1 (es) |
FI (1) | FI7846U1 (es) |
GE (3) | GEP20074022B (es) |
HK (5) | HK1072366A1 (es) |
HU (4) | HUE027004T2 (es) |
IL (5) | IL163990A0 (es) |
LT (3) | LT2425821T (es) |
MA (2) | MA27116A1 (es) |
MX (2) | MXPA04009713A (es) |
NZ (1) | NZ535286A (es) |
PH (1) | PH12018000176A1 (es) |
PT (5) | PT2425824T (es) |
RU (3) | RU2295344C2 (es) |
SI (5) | SI2425824T1 (es) |
TN (1) | TNSN04192A1 (es) |
TW (3) | TWI337077B (es) |
WO (2) | WO2003084520A2 (es) |
ZA (2) | ZA200407267B (es) |
Families Citing this family (140)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
RS50070B (sr) | 1997-12-22 | 2009-01-22 | Euro-Celtique S.A., | Oralni dozni oblik sa kombinacijom opijatnog agonista i antagonista |
US6375957B1 (en) | 1997-12-22 | 2002-04-23 | Euro-Celtique, S.A. | Opioid agonist/opioid antagonist/acetaminophen combinations |
ATE526950T1 (de) | 1999-10-29 | 2011-10-15 | Euro Celtique Sa | Hydrocodon-formulierungen mit gesteuerter freisetzung |
US10179130B2 (en) | 1999-10-29 | 2019-01-15 | Purdue Pharma L.P. | Controlled release hydrocodone formulations |
EP2517710B1 (en) | 2000-02-08 | 2015-03-25 | Euro-Celtique S.A. | Tamper-resistant oral opioid agonist formulations |
AUPQ899700A0 (en) | 2000-07-25 | 2000-08-17 | Borody, Thomas Julius | Probiotic recolonisation therapy |
EP2263658A1 (en) | 2000-10-30 | 2010-12-22 | Euro-Celtique S.A. | Controlled release hydrocodone formulations |
US20110104214A1 (en) | 2004-04-15 | 2011-05-05 | Purdue Pharma L.P. | Once-a-day oxycodone formulations |
CN1525851A (zh) | 2001-05-11 | 2004-09-01 | ������ҩ������˾ | 抗滥用阿片样物质控释剂型 |
ATE419039T1 (de) | 2001-07-18 | 2009-01-15 | Euro Celtique Sa | Pharmazeutische kombinationen von oxycodon und naloxon |
DE60232417D1 (de) | 2001-08-06 | 2009-07-02 | Euro Celtique Sa | Opioid-agonist-formulierungen mit freisetzbarem und sequestriertem antagonist |
DK2425824T5 (en) | 2002-04-05 | 2018-02-12 | Mundipharma As | Pharmaceutical preparation containing oxycodone and naloxone |
US7776314B2 (en) | 2002-06-17 | 2010-08-17 | Grunenthal Gmbh | Abuse-proofed dosage system |
MY142204A (en) | 2002-07-25 | 2010-10-29 | Pharmacia Corp | Pramipexole once-daily dosage form |
MY135852A (en) | 2003-04-21 | 2008-07-31 | Euro Celtique Sa | Pharmaceutical products |
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 |
DE10361596A1 (de) | 2003-12-24 | 2005-09-29 | Grünenthal GmbH | Verfahren zur Herstellung einer gegen Missbrauch gesicherten 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 |
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