KR890001521A - 서방형 신규 제약 제제물 - Google Patents

서방형 신규 제약 제제물 Download PDF

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Publication number
KR890001521A
KR890001521A KR870007169A KR870007169A KR890001521A KR 890001521 A KR890001521 A KR 890001521A KR 870007169 A KR870007169 A KR 870007169A KR 870007169 A KR870007169 A KR 870007169A KR 890001521 A KR890001521 A KR 890001521A
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South Korea
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formulation
active compound
solubilizer
weight
nonionic
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KR870007169A
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English (en)
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KR950002147B1 (ko
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칼-에릭 레나르트 팔크
스벤 모르간 후고손
아담 로신스키
존 알베르트 스죄그렌
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원본미기재
악티에볼라게트 헤슬레
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    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K9/00Medicinal preparations characterised by special physical form
    • A61K9/48Preparations in capsules, e.g. of gelatin, of chocolate
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K9/00Medicinal preparations characterised by special physical form
    • A61K9/20Pills, tablets, discs, rods
    • A61K9/2004Excipients; Inactive ingredients
    • A61K9/2013Organic compounds, e.g. phospholipids, fats
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435Heterocyclic 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
    • A61K31/44Non condensed pyridines; Hydrogenated derivatives thereof
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K9/00Medicinal preparations characterised by special physical form
    • A61K9/14Particulate form, e.g. powders, Processes for size reducing of pure drugs or the resulting products, Pure drug nanoparticles
    • A61K9/16Agglomerates; Granulates; Microbeadlets ; Microspheres; Pellets; Solid products obtained by spray drying, spray freeze drying, spray congealing,(multiple) emulsion solvent evaporation or extraction
    • A61K9/1605Excipients; Inactive ingredients
    • A61K9/1617Organic compounds, e.g. phospholipids, fats
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K9/00Medicinal preparations characterised by special physical form
    • A61K9/20Pills, tablets, discs, rods
    • A61K9/2004Excipients; Inactive ingredients
    • A61K9/2022Organic macromolecular compounds
    • A61K9/205Polysaccharides, e.g. alginate, gums; Cyclodextrin
    • A61K9/2054Cellulose; Cellulose derivatives, e.g. hydroxypropyl methylcellulose

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  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Veterinary Medicine (AREA)
  • Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Epidemiology (AREA)
  • Public Health (AREA)
  • General Health & Medical Sciences (AREA)
  • Biophysics (AREA)
  • Molecular Biology (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Medicinal Preparation (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Saccharide Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)

Abstract

내용 없음

Description

서방형 신규 제약 제제물
본 내용은 요부공개 건이므로 전문내용을 수록하지 않았음
제1도는 실시예 1,4 및 참조예 A에 의한 조성물이 평균 플라스마 값을 나타내는 그래프임
제2도는 실시예 3 및 참조에 B에 의한 조성물의 평균 플라스마 갑을 나타내는 그래프임,
제3도는 실시예 5에 의한 조성물 및 니페디핀을 함유하는 참조 제제물, 즉 AdalatR10mg(참조예 C)의 평균 플라스마 값을 나타내는 그래프임.

Claims (17)

  1. 반고상 또는 액상 비이온성 가용화제 중에 용해시키거나 분산시킨 유효 화합물을 함유시키되, 가용화제의 양(중량)을 유효 화합물의 양(중량과 적어도 동일하게 함을 특징으로 하는, 매우 낮은 용해도를 갖는 유효 화합물의 서방형 고상 제제물.
  2. 제1항에 있어서, 비이온성 가용화제를 폴리에틸렌글리콜의 에스테르 및 (또는) 에테르 중에서 선택한 제제물.
  3. 제1항 또는 제2항에 있어서, 비이온성 가용화제를 폴리에톡실화 지방산, 히드록실화 지방산 또는 지방 알코올 중에서 선택한 제제물.
  4. 제1항 내지 제3항 중 어느 하나의 항에 있어서, 비이온성 가용화제를 폴리에톡실화 피마자유, 폴리에톡실화 수소첨가 피마자유,피마자유로부터 채취한 폴리에톡실화 지방산 수소첨가 피마자유로부터 채취한 폴리에톡실화 지방산 중에서 선택한 제제물.
  5. 제4항에 있어서, 비이온성 가용화제가 수소첨가 피마자유 지방산과 옥시에틸화 글리세린과의 에스테르, 특히 CremophorRRH 40(바스프 제품)인 제제물.
  6. 제1항에 있어서, 유효 화합물과 가용화제의 비율이 1:1 내지 1:10 적합하기로는 1:2 내지 1:6인 제제물.
  7. 제1항 내지 제6항 중 어느 한 항에 있어서, 유효 화합물이 물 중에서 1:1000(중량) 이하의 용해도를 갖고, 비이온성 가용화제 또는 물과 비이온성 가용화제의 복합물 중에서 가용화될 수 있는 제제물.
  8. 제1항 내지 제7항 중 어느 하나의 항에 있어서, 유효 화합물이 1개 이상의 치환 디히드로피리딘류로 되는 제제물.
  9. 제8항에 있어서, 치환 디히드로피리딘이 니페디핀인 제제물.
  10. 재8항에 있어서, 치환 디히드로피리딘이 펠로디핀인 제제물.
  11. 제1항 내지 제10항중 어느 한 항에 있어서, 방출을 불활성이고 다공성인 기질, 확산 지연 코우팅 또는 붕해 코우팅에 의해 조절시킨 제제물.
  12. 제1항 내지 제10항 중 어느 하나의 항에 있어서, 방출을 친수성 겔 시스템에 의해 조절시킨 제제물.
  13. 제12항에 있어서, 친수성 겔 형성 성분이 제제물의 20%-80% 중량%로 되는 제제물.
  14. 제12항 또는 제13항에 있어서, 친수성 겔 시스템이 히드록시프로필 메틸셀룰로오스로 되는 제제물.
  15. 제14항에 있어서, 히드록시프로필 메틸세룰로오스가 4%-12중량%의 히드록시프로필 함량을 갖는 제제물.
  16. 제12항 내지 제14항 중 어느 하나의 항에 있어서, 친수성 겔 시스템에 카르복시폴리에틸렌을 함유시킨 제제물.
  17. 유효 화합물을 적어도 유효 화합물과 등량(중량)의 반고상 또는 액상 비이온성 가용화제 중에 용해 또는 분산시킨 후, 혼합물을 공지된 방법으로 적합한 서방형 시스템 중에 혼입시킨 다음, 제약 투여 단위로 제제하는 것을 특징으로 하는, 매우 낮은 용해도를 갖는 유효 화합물의 서방형 고상 제제물의 제조방법.
    ※ 참고사항 : 최초출원 내용에 의하여 공개하는 것임
KR1019870007169A 1986-04-11 1987-07-06 서방형 신규 제약 제제 KR950002147B1 (ko)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
SE8601624A SE8601624D0 (sv) 1986-04-11 1986-04-11 New pharmaceutical preparations
SE8601624-3 1986-04-11

Publications (2)

Publication Number Publication Date
KR890001521A true KR890001521A (ko) 1989-03-27
KR950002147B1 KR950002147B1 (ko) 1995-03-14

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KR870003416A KR870009720A (ko) 1986-04-11 1987-04-10 서방형 신규 제약 제제물
KR1019870007169A KR950002147B1 (ko) 1986-04-11 1987-07-06 서방형 신규 제약 제제

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KR870003416A KR870009720A (ko) 1986-04-11 1987-04-10 서방형 신규 제약 제제물

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US (1) US4803081A (ko)
EP (1) EP0249587B1 (ko)
JP (1) JPH0778016B2 (ko)
KR (2) KR870009720A (ko)
CN (1) CN1025150C (ko)
AT (1) ATE76288T1 (ko)
AU (1) AU602677B2 (ko)
CA (1) CA1304294C (ko)
CS (1) CS270560B2 (ko)
CY (1) CY1826A (ko)
DD (1) DD263231A5 (ko)
DE (1) DE3779183D1 (ko)
DK (1) DK173033B1 (ko)
DZ (1) DZ1067A1 (ko)
EG (1) EG18265A (ko)
ES (1) ES2031929T3 (ko)
FI (1) FI91826C (ko)
GR (1) GR3005286T3 (ko)
HK (1) HK26795A (ko)
HU (1) HU204699B (ko)
IE (1) IE59419B1 (ko)
IS (1) IS1553B (ko)
MY (1) MY101553A (ko)
NO (1) NO174795B (ko)
NZ (1) NZ219633A (ko)
PH (1) PH22494A (ko)
PL (1) PL265078A1 (ko)
PT (1) PT84663B (ko)
SE (1) SE8601624D0 (ko)
SG (1) SG4295G (ko)
SU (1) SU1743332A3 (ko)
UA (1) UA12336A (ko)
YU (1) YU47258B (ko)
ZA (1) ZA871911B (ko)

Families Citing this family (78)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE3720757A1 (de) * 1987-06-24 1989-01-05 Bayer Ag Dhp-manteltablette
NO883326L (no) * 1987-08-11 1989-02-13 Bayer Ag Dhp-retard-tilberedning.
DE3738236A1 (de) * 1987-11-11 1989-05-24 Euro Celtique Sa Beisskapsel
GB2222770B (en) * 1988-09-16 1992-07-29 Sandoz Ltd Pharmaceutical compositions containing cyclosporins
US6007840A (en) * 1988-09-16 1999-12-28 Novartis Ag Pharmaceutical compositions comprising cyclosporins
US4946684A (en) * 1989-06-20 1990-08-07 American Home Products Corporation Fast dissolving dosage forms
US5006344A (en) * 1989-07-10 1991-04-09 E. R. Squibb & Sons, Inc. Fosinopril tablet formulations
HU208491B (en) * 1990-11-27 1993-11-29 Gyogyszerkutato Intezet Process for producing oral pharmaceutical composition containing cyclosporin
US6262022B1 (en) 1992-06-25 2001-07-17 Novartis Ag Pharmaceutical compositions containing cyclosporin as the active agent
US5834496A (en) * 1991-12-02 1998-11-10 Sepracor, Inc. Methods for treating hypertension using optically pure S(-) felodipine
US5681812A (en) * 1991-12-10 1997-10-28 Rush Presbyterian-St. Luke's Medical Center Methods and compositions for reducing multidrug resistance
AU3243393A (en) * 1991-12-10 1993-07-19 Rush - Presbyterian - St. Luke's Medical Center Methods and compositions for reducing multi-drug resistance
GB9200607D0 (en) * 1992-01-13 1992-03-11 Ethical Pharma Ltd Pharmaceutical compositions containing nifedipine and process for the preparation thereof
JP3631490B2 (ja) 1992-05-13 2005-03-23 ノバルティス ファーマ株式会社 シクロスポリン含有眼科用組成物
US5472711A (en) * 1992-07-30 1995-12-05 Edward Mendell Co., Inc. Agglomerated hydrophilic complexes with multi-phasic release characteristics
DK0661045T3 (da) 1992-09-18 2002-10-28 Yamanouchi Pharma Co Ltd Hydrogelpræparat med forsinket frigivelse
JP3598049B2 (ja) * 1992-09-18 2004-12-08 山之内製薬株式会社 ハイドロゲル徐放性製剤
DK0589843T3 (da) 1992-09-25 2002-04-02 Novartis Ag Cyclosporinholdige farmaceutiske præparater
BE1006990A5 (nl) * 1993-04-22 1995-02-07 Univ Gent Werkwijze en samenstelling om een aktief bestanddeel in een vaste toedieningsvorm te brengen.
US5455046A (en) * 1993-09-09 1995-10-03 Edward Mendell Co., Inc. Sustained release heterodisperse hydrogel systems for insoluble drugs
US5773025A (en) * 1993-09-09 1998-06-30 Edward Mendell Co., Inc. Sustained release heterodisperse hydrogel systems--amorphous drugs
US6726930B1 (en) * 1993-09-09 2004-04-27 Penwest Pharmaceuticals Co. Sustained release heterodisperse hydrogel systems for insoluble drugs
US6129930A (en) 1993-09-20 2000-10-10 Bova; David J. Methods and sustained release nicotinic acid compositions for treating hyperlipidemia at night
US20060263428A1 (en) * 1993-09-20 2006-11-23 Eugenio Cefali Methods for treating hyperlipidemia with intermediate release nicotinic acid compositions having unique biopharmaceutical characteristics
US6676967B1 (en) * 1993-09-20 2004-01-13 Kos Pharmaceuticals, Inc. Methods for reducing flushing in individuals being treated with nicotinic acid for hyperlipidemia
US6818229B1 (en) 1993-09-20 2004-11-16 Kos Pharmaceuticals, Inc. Intermediate release nicotinic acid compositions for treating hyperlipidemia
US6080428A (en) 1993-09-20 2000-06-27 Bova; David J. Nicotinic acid compositions for treating hyperlipidemia and related methods therefor
US6746691B2 (en) 1993-09-20 2004-06-08 Kos Pharmaceuticals, Inc. Intermediate release nicotinic acid compositions for treating hyperlipidemia having unique biopharmaceutical characteristics
DE4340781C3 (de) * 1993-11-30 2000-01-27 Novartis Ag Cyclosporin enthaltende flüssige Zubereitungen und Verfahren zu ihrer Herstellung
US5945125A (en) * 1995-02-28 1999-08-31 Temple University Controlled release tablet
US5783212A (en) * 1996-02-02 1998-07-21 Temple University--of the Commonwealth System of Higher Education Controlled release drug delivery system
US6093420A (en) 1996-07-08 2000-07-25 Edward Mendell Co., Inc. Sustained release matrix for high-dose insoluble drugs
ES2229473T3 (es) 1997-01-30 2005-04-16 Novartis Ag Composiciones farmaceuticas sin aceite que contienen ciclosporina a.
US5895663A (en) * 1997-07-31 1999-04-20 L. Perrigo Company Pseudoephedrine hydrochloride extended-release tablets
AR017512A1 (es) 1997-08-22 2001-09-12 Smithkline Beecham Corp Tabletas de metilcelulosa rapidamente desintegrables para administracion por via oral y procedimiento para prepararlas
AR016827A1 (es) 1997-08-22 2001-08-01 Smithkline Beecham Corp PROCEDIMIENTO PARA LA PREPARACIoN DE UNA TABLETA FARMACÉUTICA
US6056977A (en) * 1997-10-15 2000-05-02 Edward Mendell Co., Inc. Once-a-day controlled release sulfonylurea formulation
US6555139B2 (en) 1999-06-28 2003-04-29 Wockhardt Europe Limited Preparation of micron-size pharmaceutical particles by microfluidization
SE9902742D0 (sv) * 1999-07-20 1999-07-20 Astra Ab New pharmaceutical formultion
NZ511900A (en) * 1999-09-30 2003-06-30 Penwest Pharmaceuticals Co Sustained release matrix systems for highly soluble drugs
FR2802424B1 (fr) * 1999-12-17 2002-02-15 Adir Comprime matriciel permettant la liberation prolongee de trimetazidine apres administration par voie orale
GB0001449D0 (en) * 2000-01-21 2000-03-08 Cortendo Ab Compositions
CZ301790B6 (cs) 2000-04-11 2010-06-23 Sankyo Company Limited Farmaceutický prípravek obsahující blokátor vápníku
CA2311734C (en) 2000-04-12 2011-03-08 Bristol-Myers Squibb Company Flash-melt oral dosage formulation
WO2003079972A2 (en) 2002-02-22 2003-10-02 New River Parmaceuticals Inc. Active agent delivery systems and methods for protecting and administering active agents
SE0004671D0 (sv) * 2000-12-15 2000-12-15 Amarin Dev Ab Pharmaceutical formulation
WO2002056883A1 (en) * 2001-01-18 2002-07-25 Wockhardt Limited Preparation of micron-size felodipine particles by microfluidization
DE60219478T2 (de) * 2001-07-06 2008-01-03 Endo Pharmaceuticals Inc. Orale gabe von 6-hydroxy-oxymorphon als analgetikum
ATE376826T1 (de) * 2001-09-28 2007-11-15 Mcneil Ppc Inc Darreichungsformen zur modifizierten freisetzung
US8101209B2 (en) 2001-10-09 2012-01-24 Flamel Technologies Microparticulate oral galenical form for the delayed and controlled release of pharmaceutical active principles
TWI324074B (en) * 2001-10-09 2010-05-01 Bristol Myers Squibb Co Flashmelt oral dosage formulation
US6726931B2 (en) * 2002-04-08 2004-04-27 Standard Chem. & Pharm. Co., Ltd. Process for preparing oral sustained-release formulation of felodipine
CN100553625C (zh) 2002-04-09 2009-10-28 弗拉梅技术公司 活性成分微囊的口服混悬液
ATE407674T1 (de) 2002-04-09 2008-09-15 Flamel Tech Sa Orale pharmazeutische formulierung in form einer wässrigen suspension von mikrokapseln zur modifizierten freisetzung von amoxicillin
US20030211149A1 (en) * 2002-05-07 2003-11-13 Sherman Bernard Charles Extended release tablets comprising felodipine
JP4563642B2 (ja) * 2002-05-31 2010-10-13 ワトソン ラボラトリーズ、インコーポレイテッド 医薬製剤
FR2842736B1 (fr) 2002-07-26 2005-07-22 Flamel Tech Sa Formulation pharmaceutique orale sous forme d'une pluralite de microcapsules permettant la liberation prolongee de principe(s) actif(s) peu soluble(s)
FR2842735B1 (fr) 2002-07-26 2006-01-06 Flamel Tech Sa Microcapsules a liberation modifiee de principes actifs peu solubles pour l'administration per os
US20080051411A1 (en) * 2002-12-17 2008-02-28 Cink Russell D Salts of Fenofibric Acid and Pharmaceutical Formulations Thereof
JP2006511541A (ja) * 2002-12-17 2006-04-06 アボット ゲーエムベーハー ウント カンパニー カーゲー フェノフィブル酸、その生理学的に許容し得る塩または誘導体を含有してなる製剤
US7259186B2 (en) * 2002-12-17 2007-08-21 Abbott Laboratories Salts of fenofibric acid and pharmaceutical formulations thereof
US20050032879A1 (en) * 2003-08-07 2005-02-10 Temple Okarter Formulations and use of a beta-blocker and an ACE-inhibitor for the treatment of cardiovascular diseases
TWI372066B (en) 2003-10-01 2012-09-11 Wyeth Corp Pantoprazole multiparticulate formulations
US8987322B2 (en) * 2003-11-04 2015-03-24 Circ Pharma Research And Development Limited Pharmaceutical formulations for carrier-mediated transport statins and uses thereof
EP1750717B1 (en) * 2004-02-11 2017-07-19 Rubicon Research Private Limited Controlled release pharmaceutical compositions with improved bioavailability
KR100598326B1 (ko) * 2004-04-10 2006-07-10 한미약품 주식회사 HMG-CoA 환원효소 억제제의 경구투여용 서방형 제제및 이의 제조방법
US20080152714A1 (en) * 2005-04-08 2008-06-26 Yi Gao Pharmaceutical Formulations
DK1915137T3 (da) * 2005-08-10 2013-11-04 Add Advanced Drug Delivery Technologies Ltd Oralt præparat med kontrolleret frisætning
TW200736245A (en) * 2005-11-29 2007-10-01 Sankyo Co Acid addition salts of optically active dihydropyridine derivatives
TW200806648A (en) * 2005-11-29 2008-02-01 Sankyo Co Acid addition salts of dihydropyridine derivatives
CN101103964B (zh) * 2006-07-14 2010-09-29 海南盛科生命科学研究院 一种含有非洛地平的缓释制剂及其制备方法
US20080081067A1 (en) * 2006-10-03 2008-04-03 Gupta Manishkumar Sustained release pharmaceutical compositions of venlafaxine and process for preparation thereof
US9419566B2 (en) 2011-04-20 2016-08-16 Freescale Semiconductor, Inc. Amplifiers and related integrated circuits
CN104997750B (zh) * 2015-07-30 2018-03-20 杭州康恩贝制药有限公司 一种非洛地平缓释片及其制备方法
US9687475B1 (en) 2016-03-24 2017-06-27 Ezra Pharma Llc Extended release pharmaceutical formulations with controlled impurity levels
US9675585B1 (en) 2016-03-24 2017-06-13 Ezra Pharma Extended release pharmaceutical formulations
CN109200026B (zh) * 2017-07-03 2021-01-05 北京四环科宝制药有限公司 一种非洛地平缓释片及其制备方法
AU2019285170A1 (en) 2018-06-14 2021-01-28 Astrazeneca Uk Limited Methods for lowering blood pressure with a dihydropyridine-type calcium channel blocker pharmaceutical composition

Family Cites Families (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE2714065A1 (de) * 1977-03-30 1978-10-12 Boehringer Mannheim Gmbh Instillationszubereitung
JPS5495721A (en) * 1978-01-11 1979-07-28 Nippon Kayaku Co Ltd Nifedipine preparation
CA1146866A (en) * 1979-07-05 1983-05-24 Yamanouchi Pharmaceutical Co. Ltd. Process for the production of sustained release pharmaceutical composition of solid medical material
JPS58109412A (ja) * 1981-12-23 1983-06-29 Toa Eiyou Kagaku Kogyo Kk ニフエジピン固形製剤
DE3318649A1 (de) * 1983-05-21 1984-11-22 Bayer Ag, 5090 Leverkusen Zweiphasenformulierung
DE3400106A1 (de) * 1984-01-04 1985-07-11 Klaus-Dieter Dr. 3550 Marburg Bremecker Pharmazeutische zubereitungen mit gesteuerter arzneistoff-freisetzung
KR850700212A (ko) * 1984-03-21 1985-12-26 죠지 드모트 서방성 약제학적 캼셀제
JPS618A (ja) * 1984-06-09 1986-01-06 Sawai Seiyaku Kk ニフエジピン含有製剤
IT1178511B (it) * 1984-09-14 1987-09-09 Pharmatec Spa Procedimento per la preparazione di una forma solida per uso orale a base di nifedipina con rilascio
IT1187751B (it) * 1985-10-15 1987-12-23 Eurand Spa Procedimento per la preparazione di formulazioni solidi di nifedipina ad elevata biodisponibilita' e ad effetto prolungato e formulazioni cosi' ottenute

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FI871585A0 (fi) 1987-04-10
PH22494A (en) 1988-09-12
NO174795C (ko) 1994-07-13
ATE76288T1 (de) 1992-06-15
ES2031929T3 (es) 1993-01-01
NO871199L (no) 1987-10-12
EP0249587A1 (en) 1987-12-16
DK173033B1 (da) 1999-11-29
IS3214A7 (is) 1987-10-12
HK26795A (en) 1995-03-10
FI91826B (fi) 1994-05-13
IS1553B (is) 1994-08-10
IE870925L (en) 1987-10-11
YU40787A (sh) 1992-09-07
CN87102758A (zh) 1987-10-21
PT84663B (pt) 1989-11-30
CS270560B2 (en) 1990-07-12
SE8601624D0 (sv) 1986-04-11
EG18265A (en) 1992-12-30
DK154987D0 (da) 1987-03-26
KR870009720A (ko) 1987-11-30
IE59419B1 (en) 1994-02-23
SU1743332A3 (ru) 1992-06-23
GR3005286T3 (ko) 1993-05-24
PL265078A1 (en) 1988-07-21
PT84663A (en) 1987-05-01
KR950002147B1 (ko) 1995-03-14
DK154987A (da) 1987-10-12
DD263231A5 (de) 1988-12-28
SG4295G (en) 1995-06-16
DZ1067A1 (fr) 2004-09-13
MY101553A (en) 1991-12-17
JPH0778016B2 (ja) 1995-08-23
CA1304294C (en) 1992-06-30
NO174795B (no) 1994-04-05
NZ219633A (en) 1989-11-28
CN1025150C (zh) 1994-06-29
FI91826C (fi) 1994-08-25
HUT43786A (en) 1987-12-28
YU47258B (sh) 1995-01-31
US4803081A (en) 1989-02-07
ZA871911B (en) 1987-12-30
HU204699B (en) 1992-02-28
EP0249587B1 (en) 1992-05-20
FI871585A (fi) 1987-10-12
CS258787A2 (en) 1989-11-14
AU7004387A (en) 1987-10-15
DE3779183D1 (de) 1992-06-25
UA12336A (uk) 1996-12-25
JPS62242613A (ja) 1987-10-23
NO871199D0 (no) 1987-03-23
CY1826A (en) 1995-12-01
AU602677B2 (en) 1990-10-25

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