HK184896A - Pharmaceutical composition comprising loratadine, ibuprofen and pseudoephedrine - Google Patents
Pharmaceutical composition comprising loratadine, ibuprofen and pseudoephedrine Download PDFInfo
- Publication number
- HK184896A HK184896A HK184896A HK184896A HK184896A HK 184896 A HK184896 A HK 184896A HK 184896 A HK184896 A HK 184896A HK 184896 A HK184896 A HK 184896A HK 184896 A HK184896 A HK 184896A
- Authority
- HK
- Hong Kong
- Prior art keywords
- tablet
- composition
- hydrophilic polymer
- pseudoephedrine
- loratadine
- Prior art date
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
- A61K9/2072—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
-
- 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
- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/445—Non condensed piperidines, e.g. piperocaine
-
- 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
- A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02A—TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE
- Y02A50/00—TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE in human health protection, e.g. against extreme weather
- Y02A50/30—Against vector-borne diseases, e.g. mosquito-borne, fly-borne, tick-borne or waterborne diseases whose impact is exacerbated by climate change
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- Health & Medical Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Veterinary Medicine (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Public Health (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Epidemiology (AREA)
- Organic Chemistry (AREA)
- Pain & Pain Management (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Rheumatology (AREA)
- Biomedical Technology (AREA)
- Neurology (AREA)
- Neurosurgery (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Medicinal Preparation (AREA)
Claims (13)
- Composition pharmaceutique à libération continue, comprenant un comprimé enrobé,ou l'enrobage du comprimé se compose d'une quantité antihistaminique efficace de loratadine ou de 8-chloro-6,11-dihydro-11-(4-pipéridylidène)-5H-benzo[5,6]cyclohepta [1,2-b]pyridine et d'un polymère hydrophile et le coeur du comprimé se compose d'une quantité analgésique efficace d'ibuprofène, une quantité décongestionnante efficace de pseudoéphédrine ou son sel acceptable en pharmacie et un polymère hydrophile gonflable et où l'enrobage du comprimé et le coeur du comprimé comprennent de plus des excipients acceptables en pharmacie.
- Composition de la revendication 1, où le coeur du comprimé se compose d'ibuprofène à 10 à 55% du poids du comprimé enrobé, de pseudoéphédrine ou son sel acceptable en pharmacie à 3 à 25% du poids du comprimé enrobé et d'un polymère hydrophile à 5 à 15% du poids du coeur du comprimé.
- Composition de la revendication 2, où le coeur du comprimé comprend de plus 10 à 20% d'une charge, 0 à 5% d'un agent anti-adhérent, 0,25 à 5% d'un lubrifiant et 0,5 à 3% d'un liant.
- Composition de la revendication 3, où le polymère hydrophile est un éther cellulosique choisi parmi méthylcellulose, hydroxypropylcellulose, hydroxyméthylcellulose, hydroxyéthylcellulose, carboxyméthylcellulose, carboxyéthylcellulose et leurs mélanges et la charge est du phosphate de calcium dibasique ou son dihydrate, de la cellulose microcristalline ou du lactose ; l'agent anti-adhérent est du bioxyde de silicium ou du talc ; le lubrifiant est du stéarate de magnésium ou de l'acide stéarique ; et le liant est la povidone ou l'amidon de maïs.
- Composition de la revendication 3, où le polymère hydrophile est l'hydroxypropylméthylcellulose USP 2910 ou l'hydroxypropylméthylcellulose USP 2208 ayant une viscosité de 100 000 cps dans une solution aqueuse à 2% ; la charge est la cellulose microcristalline ; le lubrifiant est le stéarate de magnésium et le liand est la povidone.
- Composition de la revendication 1, où le coeur du comprimé comprend 120 mg de sulfate de pseudoéphédrine, 555 mg d'ibuprofène à 90%, 100 mg d'hydroxypropylméthylcellulose USP 2208 ayant une viscosité de 100 000 cps dans une solution aqueuse à 2%, 10 mg de povidone, 154 mg de cellulose microcristalline et 5 mg de stéarate de magnésium et où l'enrobage du comprimé comprend 5 mg de loratadine et 10 mg d'un mélange à 5:1 d'hydroxypropylméthylcellulose USP 2910 ayant une viscosité de 6 cps dans une solution aqueuse à 2% et du polyéthylène glycol ayant un poids moléculaire de 300-6000.
- Composition de la revendication 1, où le coeur du comprimé comprend 120 mg de sulfate de pseudoéphédrine, 155 mg d'ibuprofène 90%, 150 mg d'hydroxypropylméthylcellulose USP 2910 ayant une viscosité de 4000 cps dans une solution aqueuse à 2%, 75 mg de povidone, 148,5 mg de cellulose microcristalline, 14 mg de bioxyde de silicium et 5 mg de stéarate de magnésium et où l'enrobage du comprimé se compose de 5 mg de loratadine et de 10 mg d'un mélange à 5:1 d'hydroxypropylméthylcellulose USP 2910 ayant une viscosité de 6 cps dans une solution aqueuse à 2% et de polyéthylène glycol ayant un poids moléculaire de 300-6000.
- Composition pharmaceutique à libération continue comprenant un comprimé enrobé où l'enrobage du comprimé se compose d'une quantité antihistaminique efficace de loratadine ou 8-chloro-6,11-dihydro-11-(4-pipéridylidène)-5H-benzo[5,6]cyclohepta[1,2-b]pyridine et d'un polymère hydrophile et le coeur du comprimé se compose d'une quantité analgésique efficace d'acétaminophène, d'une quantité décongestionnante efficace de pseudoéphédrine ou son sel acceptable en pharmacie et d'un polymère hydrophile gonflable, et où l'enrobage du comprimé et le coeur du comprimé comprennent de plus des excipients pharmaceutiquement acceptables.
- Composition de la revendication 8, où le coeur du comprimé se compose d'acétaminophène à 10 à 65% du poids du comprimé enrobé, de pseudoéphédrine ou son sel acceptable en pharmacie à 3 à 35% du poids du comprimé enrobé et d'un polymère hydrophile à 5 à 15% du poids du coeur du comprimé.
- Composition de la revendication 9, où le coeur du comprimé comprend de plus 10 à 20% d'une charge, 0 à 5% d'un anti-adhérent, 0,25 à 5% d'un lubrifiant et 0 à 3% d'un liant.
- Composition de la revendication 9, où le polymère hydrophile est un éther cellulosique choisi parmi méthylcellulose, hydroxypropylcellulose, hydroxyméthylcellulose, hydroxyéthylcellulose, carboxyméthylcellulose, carboxyéthylcellulose et leurs mélanges et la charge est du phosphate de calcium dibasique ou son dihydrate, de la cellulose microcristalline ou du lactose et le lubrifiant est le stéarate de magnésium ou l'acide stéarique.
- Composition de la revendication 11, où le polymère hydrophile est l'hydroxypropylméthylcellulose USP 2910 ou est l'hydroxypropylméthylcellulose USP 2208 ayant une viscosité de 100 000 cps dans une solution aqueuse à 2%; la charge est le phosphate de calcium dibasique dihydraté; et le lubrifiant est le stéarate de magnésium et l'acide stéarique.
- Composition de la revendication 8, où le coeur du comprimé comprend 60 mg de sulfate de pseudoéphédrine, 555 mg d'acétaminophène à 90%, 48 mg d'hydroxypropylméthylcellulose USP 2910 ayant une viscosité de 4000 cps dans une solution aqueuse à 2%, 98 mg de phosphate dibasique de calcium dihydraté, 10 mg d'acide stéarique et 4 mg de stéarate de magnésium et où l'enrobage du comprimé se compose de 2,5 mg de loratadine et de 5 mg d'un mélange à 5:1 d'hydroxypropylméthylcellulose USP 2910 ayant une viscosité de 6 cps dans une solution aqueuse à 2% et de polyéthylène glycol ayant un poids moléculaire de 300-6000.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US07/346,687 US4990535A (en) | 1989-05-03 | 1989-05-03 | Pharmaceutical composition comprising loratadine, ibuprofen and pseudoephedrine |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| HK184896A true HK184896A (en) | 1996-10-11 |
Family
ID=23360584
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| HK184896A HK184896A (en) | 1989-05-03 | 1996-10-03 | Pharmaceutical composition comprising loratadine, ibuprofen and pseudoephedrine |
Country Status (13)
| Country | Link |
|---|---|
| US (2) | US4990535A (fr) |
| EP (2) | EP0396404B1 (fr) |
| JP (1) | JPH066536B2 (fr) |
| KR (1) | KR940011246B1 (fr) |
| AT (1) | ATE101517T1 (fr) |
| AU (1) | AU628986B2 (fr) |
| CA (1) | CA2054752C (fr) |
| DE (1) | DE69006628T2 (fr) |
| DK (1) | DK0396404T3 (fr) |
| ES (1) | ES2062355T3 (fr) |
| HK (1) | HK184896A (fr) |
| MX (1) | MX9203278A (fr) |
| WO (1) | WO1990013295A1 (fr) |
Families Citing this family (107)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH06506198A (ja) * | 1991-03-04 | 1994-07-14 | ワーナー−ランバート・コンパニー | 種々な剤形の非ステロイド性抗炎症剤の新規な塩/イオン対 |
| JPH069382A (ja) * | 1992-04-17 | 1994-01-18 | Takeda Chem Ind Ltd | 安定化された固型製剤およびその製造方法 |
| ZA933725B (en) * | 1992-05-28 | 1993-12-15 | Elan Corp Plc | Tablet formulation |
| US5314697A (en) * | 1992-10-23 | 1994-05-24 | Schering Corporation | Stable extended release oral dosage composition comprising loratadine and pseudoephedrine |
| EP0674527A1 (fr) * | 1992-12-21 | 1995-10-04 | The Procter & Gamble Company | Utilisation d'antipodes s(+) d'agents analgesiques dans la fabrication d'une composition de traitement de troubles respiratoires |
| ES2107235T3 (es) * | 1993-06-14 | 1997-11-16 | Janssen Pharmaceutica Nv | Tableta de liberacion prolongada, revestida con pelicula, de astemizol y pseudoefedrina. |
| US6746691B2 (en) | 1993-09-20 | 2004-06-08 | Kos Pharmaceuticals, Inc. | Intermediate release nicotinic acid compositions for treating hyperlipidemia having unique biopharmaceutical characteristics |
| US6080428A (en) | 1993-09-20 | 2000-06-27 | Bova; David J. | Nicotinic acid compositions for treating hyperlipidemia and related methods therefor |
| US6818229B1 (en) | 1993-09-20 | 2004-11-16 | Kos Pharmaceuticals, Inc. | Intermediate release nicotinic acid compositions for treating hyperlipidemia |
| US6676967B1 (en) * | 1993-09-20 | 2004-01-13 | Kos Pharmaceuticals, Inc. | Methods for reducing flushing in individuals being treated with nicotinic acid for hyperlipidemia |
| US20060263428A1 (en) * | 1993-09-20 | 2006-11-23 | Eugenio Cefali | Methods for treating hyperlipidemia with intermediate release nicotinic acid compositions having unique biopharmaceutical characteristics |
| US6129930A (en) | 1993-09-20 | 2000-10-10 | Bova; David J. | Methods and sustained release nicotinic acid compositions for treating hyperlipidemia at night |
| US7211582B1 (en) | 1994-12-30 | 2007-05-01 | Sepracor Inc. | Methods for treating urticaria using descarboethoxyloratadine |
| US7214683B1 (en) | 1994-12-30 | 2007-05-08 | Sepracor Inc. | Compositions of descarboethoxyloratadine |
| DK0812195T3 (da) * | 1995-02-28 | 2003-03-03 | Aventis Pharma Inc | Farmaceutisk sammensætning til piperidinoalkanolforbindelser |
| 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 |
| US6645988B2 (en) * | 1996-01-04 | 2003-11-11 | Curators Of The University Of Missouri | Substituted benzimidazole dosage forms and method of using same |
| US6699885B2 (en) * | 1996-01-04 | 2004-03-02 | The Curators Of The University Of Missouri | Substituted benzimidazole dosage forms and methods of using same |
| US6469009B1 (en) * | 1996-04-08 | 2002-10-22 | Ucb, S.A. | Pharmaceutical compositions for the treatment of rhinitis |
| DE69734060T2 (de) * | 1996-05-24 | 2006-06-29 | Angiotech Pharmaceuticals, Inc., Vancouver | Zubereitungen und verfahren zur behandlung oder prävention von krankheiten der körperpassagewege |
| EP0811374A1 (fr) | 1996-05-29 | 1997-12-10 | Pfizer Inc. | Formulation d'une combinaison de cetirizine et pseudoephedrine |
| CO4910128A1 (es) * | 1996-10-31 | 2000-04-24 | Schering Corp | Tratamiento del asma y compuestos utiles para este trata- miento ta combinacion y un kit de esta combinacion |
| US6160020A (en) * | 1996-12-20 | 2000-12-12 | Mcneill-Ppc, Inc. | Alkali metal and alkaline-earth metal salts of acetaminophen |
| AU776837B2 (en) * | 1997-02-07 | 2004-09-23 | Sunovion Pharmaceuticals Inc. | Lactose-free non-hygroscopic and anhydrous pharmaceutical compositions of descarboethoxyloratadine |
| TW522014B (en) * | 1997-02-07 | 2003-03-01 | Sepracor Inc | Lactose-free, non-hygroscopic and anhydrous pharmaceutical unit dosage form containing descarboethoxyloratadine |
| WO1998036738A1 (fr) * | 1997-02-20 | 1998-08-27 | Therics, Inc. | Forme galenique presentant des proprietes de dispersion rapide, ses procedes d'utilisation et son procede de preparation |
| BE1011045A3 (fr) | 1997-03-14 | 1999-04-06 | Ucb Sa | Compositions pharmaceutiques pour la liberation controlee de substances actives. |
| US7179486B1 (en) | 1997-04-01 | 2007-02-20 | Nostrum Pharmaceuticals, Inc. | Process for preparing sustained release tablets |
| US5895663A (en) * | 1997-07-31 | 1999-04-20 | L. Perrigo Company | Pseudoephedrine hydrochloride extended-release tablets |
| JP4344405B2 (ja) * | 1997-08-26 | 2009-10-14 | アベンティス・ファーマスーティカルズ・インコーポレイテッド | ピペリジノアルカノール−鬱血除去剤の組合せ用医薬組成物 |
| CA2325014C (fr) * | 1998-07-10 | 2002-05-28 | Schering Corporation | Compositions orales de 8-chloro-6,11-dihydro-11-(4-piperidylidene)-5h-benzo[5,6]cyclohepta[1,2-b]pirydine |
| PE20001070A1 (es) * | 1998-09-10 | 2000-10-19 | Schering Corp | Metodos y composiciones para tratar sinusitis, otitis media y otros desordenes relacionados usando antihistaminas |
| US6521254B2 (en) | 1998-12-07 | 2003-02-18 | J-Med Pharmaceuticals, Inc. | Single-dose antihistamine/decongestant formulations for treating rhinitis |
| KR100505899B1 (ko) * | 1999-02-23 | 2005-08-01 | 주식회사유한양행 | 로라타딘과 슈도에페드린을 함유한 캅셀제 조성물 |
| US6211246B1 (en) * | 1999-06-10 | 2001-04-03 | Mcneil-Ppc, Inc. | Rapidly absorbed liquid compositions |
| US6555139B2 (en) | 1999-06-28 | 2003-04-29 | Wockhardt Europe Limited | Preparation of micron-size pharmaceutical particles by microfluidization |
| US6100274A (en) * | 1999-07-07 | 2000-08-08 | Schering Corporation | 8-chloro-6,11-dihydro-11- ](4-piperidylidine)-5H-benzo[5,6]cyclohepta[1,2-bpyridine oral compositions |
| US6264983B1 (en) * | 1999-09-16 | 2001-07-24 | Rhodia, Inc. | Directly compressible, ultra fine acetaminophen compositions and process for producing same |
| US6267986B1 (en) | 1999-09-24 | 2001-07-31 | Ranbaxy Laboratories Limited | Process for the preparation of a controlled drug delivery system containing pseudoephedrine and a long acting antihistamine |
| US6114346A (en) * | 1999-10-22 | 2000-09-05 | Schering Corporation | Treating sleep disorders using desloratadine |
| AU2276801A (en) * | 1999-12-20 | 2001-07-03 | Schering Corporation | Extended release oral dosage composition |
| WO2001045668A2 (fr) * | 1999-12-20 | 2001-06-28 | Schering Corporation | Composition de dose orale a liberation prolongee |
| US6613357B2 (en) * | 2000-01-13 | 2003-09-02 | Osmotica Corp. | Osmotic device containing pseudoephedrine and an H1 antagonist |
| DE10003757A1 (de) * | 2000-01-28 | 2001-08-02 | Knoll Ag | Ibuprofen-Wirkstoffzubereitung |
| US7405223B2 (en) | 2000-02-03 | 2008-07-29 | Schering Corporation | Treating allergic and inflammatory conditions |
| EP1276502A1 (fr) * | 2000-04-14 | 2003-01-22 | J-Med Pharmaceuticals, Inc. | Formulations antihistaminiques/decongestionnantes a dose unique |
| ES2185452B2 (es) * | 2000-08-01 | 2004-03-16 | Cinfa S A Lab | Composicion farmaceutica de fluoxetina en comprimido dispersable recubierto y su proceso de fabricacion. |
| US20020094345A1 (en) | 2000-10-06 | 2002-07-18 | Sara Abelaira | Pharmaceutical compositions containing epinastine and pseudoephedrine |
| WO2002036077A2 (fr) * | 2000-11-06 | 2002-05-10 | Andrx Pharmaceuticals, Inc. | Preparation decongestionnante et antihistaminique a prise quotidienne unique |
| US6982251B2 (en) * | 2000-12-20 | 2006-01-03 | Schering Corporation | Substituted 2-azetidinones useful as hypocholesterolemic agents |
| CA2434169C (fr) | 2001-01-12 | 2011-03-15 | Sun Pharmaceutical Industries Limited | Systeme de liberation espacee de medicaments |
| PL364178A1 (en) * | 2001-01-26 | 2004-12-13 | Schering Corporation | Combinations of sterol absorption inhibitor(s) with blood modifier(s) for treating vascular conditions |
| HU230253B1 (hu) * | 2001-01-26 | 2015-11-30 | Merck Sharp & Dohme Corp | Peroxiszóma proliferátor-aktivált receptor (PPAR) aktivátor(ok) és szterin-abszorpció inhibitor(ok) kombinációi és alkalmazásuk vaszkuláris indikációk kezelésére |
| AU2002241956A1 (en) * | 2001-01-26 | 2002-08-06 | Schering Corporation | Combinations of bile acid sequestrant(s) and sterol absorption inhibitor(s) and treatments for vascular indications |
| US20020183305A1 (en) * | 2001-01-26 | 2002-12-05 | Schering Corporation | Combinations of nicotinic acid and derivatives thereof and sterol absorption inhibitor(s) and treatments for vascular indications |
| US20060287254A1 (en) * | 2001-01-26 | 2006-12-21 | Schering Corporation | Use of substituted azetidinone compounds for the treatment of sitosterolemia |
| IL156585A0 (en) * | 2001-01-26 | 2004-01-04 | Schering Corp | Combinations of sterol absorption inhibitor(s) with cardiovascular agent(s) for the treatment of vascular conditions |
| DK1355644T3 (da) * | 2001-01-26 | 2006-10-23 | Schering Corp | Anvendelse af substituerede azetidinonforbindelser til behandling af sitosterolæmi |
| US7071181B2 (en) * | 2001-01-26 | 2006-07-04 | Schering Corporation | Methods and therapeutic combinations for the treatment of diabetes using sterol absorption inhibitors |
| CA2443632C (fr) * | 2001-04-10 | 2011-05-03 | Sun Pharmaceutical Industries Limited | Composition a liberation par impulsion reglee dans le temps |
| JP2004532868A (ja) * | 2001-05-25 | 2004-10-28 | シェーリング コーポレイション | アルツハイマー病の処置におけるアゼチジノン置換誘導体の使用 |
| CN1518448A (zh) * | 2001-06-20 | 2004-08-04 | ���鹫˾ | 用于治疗鼻充血和鼻塞的抗组胺剂 |
| JP2005515966A (ja) * | 2001-07-06 | 2005-06-02 | エンドー ファーマシューティカルズ, インコーポレイティド | 鎮痛薬としての使用のための6−ヒドロキシ−オキシモルホンの経口投与 |
| US6720002B2 (en) | 2001-07-20 | 2004-04-13 | R.P. Scherer Technologies, Inc. | Antihistamine formulations for soft capsule dosage forms |
| US7053080B2 (en) * | 2001-09-21 | 2006-05-30 | Schering Corporation | Methods and therapeutic combinations for the treatment of obesity using sterol absorption inhibitors |
| AU2002335770B2 (en) * | 2001-09-21 | 2005-08-18 | Merck Sharp & Dohme Corp. | Methods for treating or preventing vascular inflammation using sterol absorption inhibitor(s) |
| JP2005504091A (ja) * | 2001-09-21 | 2005-02-10 | シェーリング コーポレイション | ステロール吸収阻害剤としてアゼチジノンを用いる黄色腫の処置 |
| US7056906B2 (en) * | 2001-09-21 | 2006-06-06 | Schering Corporation | Combinations of hormone replacement therapy composition(s) and sterol absorption inhibitor(s) and treatments for vascular conditions in post-menopausal women |
| US20030119808A1 (en) * | 2001-09-21 | 2003-06-26 | Schering Corporation | Methods of treating or preventing cardiovascular conditions while preventing or minimizing muscular degeneration side effects |
| US7838026B2 (en) | 2001-09-28 | 2010-11-23 | Mcneil-Ppc, Inc. | Burst-release polymer composition and dosage forms comprising the same |
| US6837696B2 (en) * | 2001-09-28 | 2005-01-04 | Mcneil-Ppc, Inc. | Apparatus for manufacturing dosage forms |
| US7122143B2 (en) | 2001-09-28 | 2006-10-17 | Mcneil-Ppc, Inc. | Methods for manufacturing dosage forms |
| NZ532096A (en) * | 2001-09-28 | 2006-10-27 | Mcneil Ppc Inc | Dosage forms having an inner core and outer shell with different shapes |
| AR040588A1 (es) * | 2002-07-26 | 2005-04-13 | Schering Corp | Formulacion farmaceutica que comprende un inhibidor de la absorcion del colesterol y un inhibidor de una hmg- co a reductasa |
| WO2004043457A1 (fr) * | 2002-11-06 | 2004-05-27 | Schering Corporation | Inhibiteurs d'absorption de cholesterol pour le traitement de troubles auto-immuns |
| US8092831B2 (en) * | 2002-11-08 | 2012-01-10 | Andrx Pharmaceuticals, Llc | Antihistamine and decongestant system |
| CL2003002653A1 (es) * | 2002-12-18 | 2005-04-22 | Wyeth Corp | Composicion farmaceutica que comprende (a) un antiinflamatorio no esteroidal (nsaid), preferentemente ibuprofeno, (b) un descongestionante, preferentemente pseudoefedrina y (c) un antihistaminico, preferentemente clorfeniramina; metodo para su prepar |
| US20040253311A1 (en) * | 2002-12-18 | 2004-12-16 | Roger Berlin | Multi-layer tablet comprising non-steroidal anti-inflammatory drugs, decongestants and non-sedating antihist amines |
| US20040142903A1 (en) * | 2003-01-16 | 2004-07-22 | Par Pharmaceutical Inc. | Bioavailable fenofibrate compositions, methods for treating hyperlipidemia and hypercholesterolemia and processes for the preparation of such compositions |
| JP4589919B2 (ja) * | 2003-03-07 | 2010-12-01 | シェーリング コーポレイション | 高コレステロール血症の処置のための、置換アゼチジノン化合物、これらの処方物および使用 |
| JP2006519869A (ja) | 2003-03-07 | 2006-08-31 | シェーリング コーポレイション | 置換アゼチジノン化合物、置換アゼチジノン化合物を調製するためのプロセス、それらの処方物および使用 |
| US7459442B2 (en) * | 2003-03-07 | 2008-12-02 | Schering Corporation | Substituted azetidinone compounds, processes for preparing the same, formulations and uses thereof |
| CA2517571C (fr) | 2003-03-07 | 2011-07-05 | Schering Corporation | Azetidinones substituees , procedes pour leur preparation, formulations et utilisations de celles-ci |
| CN100379408C (zh) * | 2003-07-28 | 2008-04-09 | 马林克罗特公司 | 改进的硬脂酸盐组合物及制备方法 |
| CA2540308C (fr) | 2003-09-26 | 2013-08-06 | Alza Corporation | Enrobage de medicaments a charge medicamenteuse elevee et procedes de fabrication |
| EP1680189A2 (fr) * | 2003-11-05 | 2006-07-19 | Schering Corporation | Combinaisons de modulateurs lipidiques et d'azetidinones substituees et traitements d'affections vasculaires |
| US20050266032A1 (en) * | 2003-12-17 | 2005-12-01 | Sovereign Pharmaceuticals, Ltd. | Dosage form containing multiple drugs |
| US8188067B2 (en) | 2004-04-01 | 2012-05-29 | Teva Pharmaceutical Industries Ltd. | Formulations of 6-mercaptopurine |
| US20060068009A1 (en) * | 2004-09-30 | 2006-03-30 | Scolr Pharma, Inc. | Modified release ibuprofen dosage form |
| US20070077297A1 (en) * | 2004-09-30 | 2007-04-05 | Scolr Pharma, Inc. | Modified release ibuprofen dosage form |
| US20070036859A1 (en) * | 2005-08-11 | 2007-02-15 | Perry Ronald L | Sustained release antihistamine and decongestant composition |
| WO2007143158A2 (fr) | 2006-06-01 | 2007-12-13 | Schering-Plough Healthcare Products, Inc. | Formulations pharmaceutiques de phényléphrine et compositions pour absorption par le côlon |
| RU2008151945A (ru) * | 2006-06-01 | 2010-07-20 | Шеринг Корпорейшн (US) | Лекарственные формы с пульсирующим высвобождением и фармацевтические композиции фенилэфрина |
| US7749537B2 (en) * | 2006-12-04 | 2010-07-06 | Scolr Pharma, Inc. | Method of forming a tablet |
| ES2590604T3 (es) * | 2008-01-04 | 2016-11-22 | Schabar Research Associates Llc | Composición que comprende un analgésico y un antihistamínico |
| US20130115250A1 (en) * | 2009-05-13 | 2013-05-09 | Wyeth Llc | Burst Drug Release Compositions |
| US20110104272A1 (en) * | 2009-11-05 | 2011-05-05 | Depomed, Inc. | Gastric retentive extended-release dosage forms comprising combinations of acetaminophen and phenylephrine |
| CA2690490C (fr) | 2010-01-19 | 2012-06-26 | Accucaps Industries Limited | Formulations pharmaceutiques de loratadine pour encapsulation et combinaisons associees |
| JP5752578B2 (ja) * | 2011-12-09 | 2015-07-22 | ジェイ−メド ファーマシューティカルズ,インコーポレーティッド | 鼻炎治療のための単一投与抗ヒスタミン薬/鬱血除去薬製剤 |
| EP2727592A1 (fr) * | 2012-11-05 | 2014-05-07 | Kücükgüzel, Sükriye Güniz | Combinaison de desloratadine et de paracétamol |
| HRP20220112T1 (hr) | 2013-12-24 | 2022-04-15 | Virginia Commonwealth University | Upotreba oksidacijskog sulfata kolesterola (ocs) za liječenje akutne insuficijencije jetre |
| US20170105996A1 (en) | 2015-10-16 | 2017-04-20 | Teva Pharmaceutical Industries, Ltd. | Treatment of non-alcoholic fatty liver disease or non-alcoholic steatohepatitis with delayed-release 6-mercaptopurine |
| 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 |
| CR20230109A (es) | 2020-07-30 | 2023-05-11 | Faes Farma Sa | Sistema de liberación de fármacos descongestivos y bilastina |
Family Cites Families (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4282233B1 (en) | 1980-06-19 | 2000-09-05 | Schering Corp | Antihistaminic 11-(4-piperidylidene)-5h-benzoÄ5,6Ü-cyclohepta-Ä1,2Ü-pyridines |
| HU194864B (en) | 1984-02-15 | 1988-03-28 | Schering Corp | Process for production of 8-chlor-6,11-dihydro-11-(4-piperidilidene)-5h-benzo (5,6)-cyclo-hepta (1,2-b) pyridine and its salts |
| US4540566A (en) * | 1984-04-02 | 1985-09-10 | Forest Laboratories, Inc. | Prolonged release drug dosage forms based on modified low viscosity grade hydroxypropylmethylcellulose |
| US4871733A (en) * | 1984-04-09 | 1989-10-03 | Analgesic Associates | Cough/cold mixtures comprising non-sedating antihistamine drugs |
| US4783465A (en) | 1984-04-09 | 1988-11-08 | Analgesic Associates | Cough/cold mixtures comprising non-sedating antihistamine drugs |
| US4552899A (en) | 1984-04-09 | 1985-11-12 | Analgesic Associates | Cough/cold mixtures comprising non-steroidal anti-inflammatory drugs |
| FR2576213B1 (fr) * | 1985-01-21 | 1989-02-24 | Cortial | Nouveau procede d'obtention de formes pharmaceutiques a liberation prolongee |
| US4829064A (en) * | 1987-06-08 | 1989-05-09 | Analgesic Associates | Cough/cold mixtures comprising non-sedating antihistamine drugs |
| US4999189A (en) * | 1988-11-14 | 1991-03-12 | Schering Corporation | Sustained release oral suspensions |
-
1989
- 1989-05-03 US US07/346,687 patent/US4990535A/en not_active Expired - Lifetime
-
1990
- 1990-05-02 AT AT90304792T patent/ATE101517T1/de not_active IP Right Cessation
- 1990-05-02 DE DE69006628T patent/DE69006628T2/de not_active Expired - Fee Related
- 1990-05-02 EP EP90304792A patent/EP0396404B1/fr not_active Expired - Lifetime
- 1990-05-02 CA CA002054752A patent/CA2054752C/fr not_active Expired - Fee Related
- 1990-05-02 DK DK90304792.6T patent/DK0396404T3/da active
- 1990-05-02 EP EP90907694A patent/EP0471009A1/fr active Pending
- 1990-05-02 ES ES90304792T patent/ES2062355T3/es not_active Expired - Lifetime
- 1990-05-02 WO PCT/US1990/002326 patent/WO1990013295A1/fr not_active Ceased
- 1990-05-02 JP JP2507797A patent/JPH066536B2/ja not_active Expired - Lifetime
- 1990-05-02 AU AU56648/90A patent/AU628986B2/en not_active Ceased
- 1990-05-02 KR KR1019900702700A patent/KR940011246B1/ko not_active Expired - Fee Related
- 1990-11-13 US US07/612,633 patent/US5100675A/en not_active Expired - Lifetime
-
1992
- 1992-06-24 MX MX9203278A patent/MX9203278A/es unknown
-
1996
- 1996-10-03 HK HK184896A patent/HK184896A/en not_active IP Right Cessation
Also Published As
| Publication number | Publication date |
|---|---|
| KR920700033A (ko) | 1992-02-19 |
| EP0396404A1 (fr) | 1990-11-07 |
| KR940011246B1 (ko) | 1994-12-03 |
| MX9203278A (es) | 1992-07-01 |
| AU5664890A (en) | 1990-11-29 |
| US4990535A (en) | 1991-02-05 |
| JPH066536B2 (ja) | 1994-01-26 |
| JPH04501425A (ja) | 1992-03-12 |
| EP0396404B1 (fr) | 1994-02-16 |
| ES2062355T3 (es) | 1994-12-16 |
| ATE101517T1 (de) | 1994-03-15 |
| US5100675A (en) | 1992-03-31 |
| WO1990013295A1 (fr) | 1990-11-15 |
| DK0396404T3 (da) | 1994-03-14 |
| CA2054752C (fr) | 1996-12-31 |
| AU628986B2 (en) | 1992-09-24 |
| CA2054752A1 (fr) | 1990-11-04 |
| EP0471009A1 (fr) | 1992-02-19 |
| DE69006628D1 (de) | 1994-03-24 |
| DE69006628T2 (de) | 1994-05-26 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| PC | Patent ceased (i.e. patent has lapsed due to the failure to pay the renewal fee) |