NO310495B1 - Farmasöytiske blandinger inneholdende irbesartan - Google Patents
Farmasöytiske blandinger inneholdende irbesartan Download PDFInfo
- Publication number
- NO310495B1 NO310495B1 NO19962387A NO962387A NO310495B1 NO 310495 B1 NO310495 B1 NO 310495B1 NO 19962387 A NO19962387 A NO 19962387A NO 962387 A NO962387 A NO 962387A NO 310495 B1 NO310495 B1 NO 310495B1
- Authority
- NO
- Norway
- Prior art keywords
- weight
- irbesartan
- hydrochlorothiazide
- diuretic
- sodium
- Prior art date
Links
- 239000002947 C09CA04 - Irbesartan Substances 0.000 title claims description 50
- 229960002198 irbesartan Drugs 0.000 title claims description 50
- YCPOHTHPUREGFM-UHFFFAOYSA-N irbesartan Chemical compound O=C1N(CC=2C=CC(=CC=2)C=2C(=CC=CC=2)C=2[N]N=NN=2)C(CCCC)=NC21CCCC2 YCPOHTHPUREGFM-UHFFFAOYSA-N 0.000 title claims description 50
- 239000008194 pharmaceutical composition Substances 0.000 title description 4
- 239000000203 mixture Substances 0.000 claims description 77
- JZUFKLXOESDKRF-UHFFFAOYSA-N Chlorothiazide Chemical compound C1=C(Cl)C(S(=O)(=O)N)=CC2=C1NCNS2(=O)=O JZUFKLXOESDKRF-UHFFFAOYSA-N 0.000 claims description 35
- 229960002003 hydrochlorothiazide Drugs 0.000 claims description 33
- 239000002934 diuretic Substances 0.000 claims description 32
- 230000001882 diuretic effect Effects 0.000 claims description 31
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims description 18
- HQKMJHAJHXVSDF-UHFFFAOYSA-L magnesium stearate Chemical compound [Mg+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O HQKMJHAJHXVSDF-UHFFFAOYSA-L 0.000 claims description 18
- DPXJVFZANSGRMM-UHFFFAOYSA-N acetic acid;2,3,4,5,6-pentahydroxyhexanal;sodium Chemical compound [Na].CC(O)=O.OCC(O)C(O)C(O)C(O)C=O DPXJVFZANSGRMM-UHFFFAOYSA-N 0.000 claims description 15
- 150000001875 compounds Chemical class 0.000 claims description 15
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- 239000011230 binding agent Substances 0.000 claims description 11
- UQSXHKLRYXJYBZ-UHFFFAOYSA-N iron oxide Inorganic materials [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 claims description 11
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- 229940016286 microcrystalline cellulose Drugs 0.000 claims description 11
- 235000019813 microcrystalline cellulose Nutrition 0.000 claims description 11
- GUBGYTABKSRVRQ-XLOQQCSPSA-N Alpha-Lactose Chemical compound O[C@@H]1[C@@H](O)[C@@H](O)[C@@H](CO)O[C@H]1O[C@@H]1[C@@H](CO)O[C@H](O)[C@H](O)[C@H]1O GUBGYTABKSRVRQ-XLOQQCSPSA-N 0.000 claims description 10
- 229920002785 Croscarmellose sodium Polymers 0.000 claims description 10
- 229960001681 croscarmellose sodium Drugs 0.000 claims description 10
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- 239000000314 lubricant Substances 0.000 claims description 10
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- WHNWPMSKXPGLAX-UHFFFAOYSA-N N-Vinyl-2-pyrrolidone Chemical compound C=CN1CCCC1=O WHNWPMSKXPGLAX-UHFFFAOYSA-N 0.000 claims description 7
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- IXPNQXFRVYWDDI-UHFFFAOYSA-N 1-methyl-2,4-dioxo-1,3-diazinane-5-carboximidamide Chemical compound CN1CC(C(N)=N)C(=O)NC1=O IXPNQXFRVYWDDI-UHFFFAOYSA-N 0.000 claims description 4
- VBICKXHEKHSIBG-UHFFFAOYSA-N 1-monostearoylglycerol Chemical compound CCCCCCCCCCCCCCCCCC(=O)OCC(O)CO VBICKXHEKHSIBG-UHFFFAOYSA-N 0.000 claims description 4
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- 150000004781 alginic acids Chemical class 0.000 claims description 4
- 229960004977 anhydrous lactose Drugs 0.000 claims description 4
- LDHBWEYLDHLIBQ-UHFFFAOYSA-M iron(3+);oxygen(2-);hydroxide;hydrate Chemical compound O.[OH-].[O-2].[Fe+3] LDHBWEYLDHLIBQ-UHFFFAOYSA-M 0.000 claims description 4
- YOBAEOGBNPPUQV-UHFFFAOYSA-N iron;trihydrate Chemical compound O.O.O.[Fe].[Fe] YOBAEOGBNPPUQV-UHFFFAOYSA-N 0.000 claims description 4
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- DBMJMQXJHONAFJ-UHFFFAOYSA-M Sodium laurylsulphate Chemical compound [Na+].CCCCCCCCCCCCOS([O-])(=O)=O DBMJMQXJHONAFJ-UHFFFAOYSA-M 0.000 claims description 3
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- CJZGTCYPCWQAJB-UHFFFAOYSA-L calcium stearate Chemical compound [Ca+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O CJZGTCYPCWQAJB-UHFFFAOYSA-L 0.000 claims description 2
- 239000008116 calcium stearate Substances 0.000 claims description 2
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- GXGAKHNRMVGRPK-UHFFFAOYSA-N dimagnesium;dioxido-bis[[oxido(oxo)silyl]oxy]silane Chemical compound [Mg+2].[Mg+2].[O-][Si](=O)O[Si]([O-])([O-])O[Si]([O-])=O GXGAKHNRMVGRPK-UHFFFAOYSA-N 0.000 claims description 2
- MVPICKVDHDWCJQ-UHFFFAOYSA-N ethyl 3-pyrrolidin-1-ylpropanoate Chemical compound CCOC(=O)CCN1CCCC1 MVPICKVDHDWCJQ-UHFFFAOYSA-N 0.000 claims description 2
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Classifications
-
- 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
- A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
- A61K31/425—Thiazoles
-
- 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
- A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
- A61K31/415—1,2-Diazoles
-
- 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
- A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
- A61K31/4164—1,3-Diazoles
- A61K31/4178—1,3-Diazoles not condensed 1,3-diazoles and containing further heterocyclic rings, e.g. pilocarpine, nitrofurantoin
-
- 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
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
-
- 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
- A61K31/54—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one sulfur as the ring hetero atoms, e.g. sulthiame
-
- 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
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P13/00—Drugs for disorders of the urinary system
-
- 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
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P7/00—Drugs for disorders of the blood or the extracellular fluid
- A61P7/10—Antioedematous agents; Diuretics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/04—Inotropic agents, i.e. stimulants of cardiac contraction; Drugs for heart failure
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/12—Antihypertensives
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- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Veterinary Medicine (AREA)
- Chemical & Material Sciences (AREA)
- Public Health (AREA)
- Medicinal Chemistry (AREA)
- General Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Pharmacology & Pharmacy (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Epidemiology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Cardiology (AREA)
- Heart & Thoracic Surgery (AREA)
- Hospice & Palliative Care (AREA)
- Hematology (AREA)
- Diabetes (AREA)
- Urology & Nephrology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Medicinal Preparation (AREA)
- Plural Heterocyclic Compounds (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US47261895A | 1995-06-07 | 1995-06-07 |
Publications (3)
Publication Number | Publication Date |
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NO962387D0 NO962387D0 (no) | 1996-06-06 |
NO962387L NO962387L (no) | 1996-12-09 |
NO310495B1 true NO310495B1 (no) | 2001-07-16 |
Family
ID=23876256
Family Applications (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
NO19962387A NO310495B1 (no) | 1995-06-07 | 1996-06-06 | Farmasöytiske blandinger inneholdende irbesartan |
NO20004743A NO310393B1 (no) | 1995-06-07 | 2000-09-22 | Farmasöytiske blandinger inneholdende irbesartan og et diuretikum |
Family Applications After (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
NO20004743A NO310393B1 (no) | 1995-06-07 | 2000-09-22 | Farmasöytiske blandinger inneholdende irbesartan og et diuretikum |
Country Status (23)
Country | Link |
---|---|
EP (2) | EP0747050B2 (cs) |
JP (1) | JP3162626B2 (cs) |
KR (1) | KR100442719B1 (cs) |
CN (1) | CN1149083C (cs) |
AR (2) | AR002350A1 (cs) |
AT (2) | ATE503478T1 (cs) |
AU (1) | AU702651B2 (cs) |
CA (1) | CA2177772C (cs) |
CZ (1) | CZ291532B6 (cs) |
DE (2) | DE69629755T3 (cs) |
DK (2) | DK1275391T3 (cs) |
ES (2) | ES2363127T3 (cs) |
HK (1) | HK1002384A1 (cs) |
HU (1) | HU229369B1 (cs) |
IL (1) | IL118309A (cs) |
NO (2) | NO310495B1 (cs) |
NZ (2) | NZ286612A (cs) |
PL (1) | PL184893B1 (cs) |
PT (2) | PT1275391E (cs) |
RU (2) | RU2181590C2 (cs) |
SG (1) | SG49956A1 (cs) |
TW (1) | TW442301B (cs) |
ZA (1) | ZA964337B (cs) |
Families Citing this family (56)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2000004862A2 (en) * | 1998-07-20 | 2000-02-03 | Smithkline Beecham Corporation | Bioenhanced formulations comprising eprosartan in oral solid dosage form |
SE9903028D0 (sv) * | 1999-08-27 | 1999-08-27 | Astra Ab | New use |
JP4565456B2 (ja) * | 1999-11-02 | 2010-10-20 | 塩野義製薬株式会社 | 着色顆粒の色素定着法 |
GB0001621D0 (en) * | 2000-01-26 | 2000-03-15 | Astrazeneca Ab | Pharmaceutical compositions |
CA2311734C (en) * | 2000-04-12 | 2011-03-08 | Bristol-Myers Squibb Company | Flash-melt oral dosage formulation |
GB0209265D0 (en) | 2002-04-23 | 2002-06-05 | Novartis Ag | Organic compounds |
US8980870B2 (en) | 2002-09-24 | 2015-03-17 | Boehringer Ingelheim International Gmbh | Solid telmisartan pharmaceutical formulations |
DE10244681A1 (de) * | 2002-09-24 | 2004-04-08 | Boehringer Ingelheim International Gmbh | Neue feste Telmisartan enthaltende pharmazeutische Formulierungen und deren Herstellung |
EP1648515B1 (en) * | 2003-07-16 | 2012-11-21 | Boehringer Ingelheim International GmbH | Chlorthalidone combinations |
TR200301553A1 (tr) * | 2003-09-18 | 2005-10-21 | Nobel �La� Sanay�� Ve T�Caret A.�. | İrbesartan etken maddesi içeren yeni oral farmasötik formülasyonlar |
JP2005126338A (ja) * | 2003-10-21 | 2005-05-19 | Boehringer Ingelheim Pharma Gmbh & Co Kg | 心不全治療剤 |
WO2005089720A1 (en) * | 2004-03-10 | 2005-09-29 | Ranbaxy Laboratories Limited | Valsartan tablets and the process for the preparation thereof |
DE602005025755D1 (de) | 2004-06-04 | 2011-02-17 | Teva Pharma | Irbesartan enthaltende pharmazeutische zusammensetzung |
WO2006013545A1 (en) * | 2004-07-28 | 2006-02-09 | Ranbaxy Laboratories Limited | Pharmaceutical compositions of irbesartan |
WO2007031933A2 (en) | 2005-09-12 | 2007-03-22 | Actelion Pharmaceuticals Ltd | Stable pharmaceutical composition comprising a pyrimidine-sulfamide |
WO2007061829A2 (en) * | 2005-11-17 | 2007-05-31 | Novartis Ag | Pharmaceutical composition |
PT1806130E (pt) * | 2006-01-09 | 2010-05-11 | Krka D D Novo Mesto | Composições farmacêuticas sólidas que compreendem irbesartan |
DE102006006588A1 (de) * | 2006-02-13 | 2007-08-16 | Ratiopharm Gmbh | Schnell freisetzende Irbesartan-haltige pharmazeutische Zusammensetzung |
KR20090024248A (ko) | 2006-06-12 | 2009-03-06 | 쉐링 코포레이션 | Cxcr2의 선택적 길항제 또는 cxcr1과 cxcr2 둘다의 선택적 길항제의 약제학적 제형 및 조성물, 및 염증성 질환을 치료하기 위한 이의 사용방법 |
CA2654890C (en) | 2006-06-16 | 2015-10-06 | Lek Pharmaceuticals D.D. | Pharmaceutical composition |
GB0612540D0 (en) * | 2006-06-23 | 2006-08-02 | Novartis Ag | Galenical formulations of organic compounds |
EP1923053A1 (en) * | 2006-09-27 | 2008-05-21 | Novartis AG | Pharmaceutical compositions comprising nilotinib or its salt |
RU2465900C2 (ru) * | 2007-04-17 | 2012-11-10 | Рациофарм Гмбх | Фармацевтические композиции, содержащие ирбесартан |
JP5683058B2 (ja) * | 2007-04-27 | 2015-03-11 | ニプロ株式会社 | 経口固形製剤及びその製造方法 |
TR200703568A1 (tr) | 2007-05-24 | 2008-07-21 | Sanovel �La� Sanay� Ve T�Caret Anon�M ��Rket� | Valsartan formülasyonları |
MX2010001837A (es) | 2007-08-17 | 2010-03-10 | Actelion Pharmaceuticals Ltd | Derivados de 4-pirimidinasulfamida. |
PL2065035T3 (pl) | 2007-11-28 | 2011-02-28 | Lesvi Laboratorios Sl | Preparaty farmaceutyczne zawierające irbesartan |
CN101327213B (zh) * | 2008-06-20 | 2010-10-13 | 海南锦瑞制药股份有限公司 | 厄贝沙坦氢氯噻嗪药用组合物及其制备方法 |
JP5296456B2 (ja) * | 2008-08-26 | 2013-09-25 | 大日本住友製薬株式会社 | 溶出が良好なイルベサルタン含有医薬組成物および口腔内崩壊錠 |
WO2010075347A2 (en) * | 2008-12-23 | 2010-07-01 | Takeda Pharmaceutical Company Limited | Methods of treating hypertension with at least one angiotensin ii receptor blocker and chlorthalidone |
PL2448561T3 (pl) * | 2009-06-30 | 2014-01-31 | Sanofi Sa | Stałe kompozycje farmaceutyczne o ustalonej dawce, zawierające irbesartan i amlodypinę, ich wytwarzanie oraz ich zastosowanie terapeutyczne |
WO2011010316A1 (en) * | 2009-07-20 | 2011-01-27 | Hetero Research Foundation | Pharmaceutical compositions of irbesartan |
PT2498756T (pt) * | 2009-11-09 | 2019-11-26 | Wyeth Llc | Formulações de comprimidos de maleato de neratinib |
ES2364011B1 (es) | 2009-11-20 | 2013-01-24 | Gp Pharm, S.A. | Cápsulas de principios activos farmacéuticos y ésteres de ácidos grasos poliinsaturados para el tratamiento de enfermedades cardiovasculares. |
JP4974255B2 (ja) * | 2010-03-16 | 2012-07-11 | 塩野義製薬株式会社 | アンジオテンシンii受容体拮抗剤の配合剤 |
JP5459670B2 (ja) * | 2010-05-07 | 2014-04-02 | 塩野義製薬株式会社 | 着色顆粒の色素定着化剤 |
US20120010216A1 (en) * | 2010-07-06 | 2012-01-12 | Brown Arthur M | Pharmaceutical compositions containing vanoxerine |
US8703203B2 (en) * | 2010-07-08 | 2014-04-22 | Ratiopharm Gmbh | Oral dosage form of deferasirox |
WO2013100112A1 (ja) * | 2011-12-28 | 2013-07-04 | ニプロ株式会社 | アンギオテンシンii拮抗作用を有する化合物を含有する固形医薬組成物 |
DK2851075T3 (da) | 2012-05-14 | 2022-01-31 | Shionogi & Co | Præparat, der indeholder 6,7-umættet -7-carbamoylmorphinanderivat |
HUE051406T2 (hu) | 2012-11-14 | 2021-03-01 | Grace W R & Co | Biológiailag aktív anyagot és rendezetlen szervetlen oxidot tartalmazó kompozíciók |
JP5714652B2 (ja) * | 2013-06-13 | 2015-05-07 | 大日本住友製薬株式会社 | 溶出が良好なイルベサルタン含有医薬組成物および口腔内崩壊錠 |
JP6238921B2 (ja) * | 2014-02-17 | 2017-11-29 | 大原薬品工業株式会社 | イルベサルタンを含有する錠剤 |
JP5978335B2 (ja) * | 2015-03-11 | 2016-08-24 | 大日本住友製薬株式会社 | 溶出が良好なイルベサルタン含有医薬組成物および口腔内崩壊錠 |
JP6199922B2 (ja) * | 2015-03-20 | 2017-09-20 | 大原薬品工業株式会社 | 化学的な安定性が向上したイルベサルタン含有錠剤 |
JP6445923B2 (ja) * | 2015-04-22 | 2018-12-26 | ダイト株式会社 | イルベサルタン含有錠剤の調製方法 |
JP6737060B2 (ja) * | 2015-09-11 | 2020-08-05 | ニプロ株式会社 | イルベサルタンを含有する医薬組成物の製造方法 |
JP6151413B2 (ja) * | 2016-07-25 | 2017-06-21 | 大日本住友製薬株式会社 | 溶出が良好なイルベサルタン含有医薬組成物および口腔内崩壊錠 |
JP2017141299A (ja) * | 2017-05-24 | 2017-08-17 | 大日本住友製薬株式会社 | 溶出が良好なイルベサルタン含有医薬組成物および口腔内崩壊錠 |
JP6233911B2 (ja) * | 2017-08-22 | 2017-11-22 | 大原薬品工業株式会社 | 化学的な安定性が向上したイルベサルタン含有錠剤 |
JP2018009032A (ja) * | 2017-10-19 | 2018-01-18 | 大原薬品工業株式会社 | 化学的な安定性が向上したイルベサルタン含有錠剤 |
CN108434112A (zh) * | 2018-06-08 | 2018-08-24 | 华益药业科技(安徽)有限公司 | 一种厄贝沙坦片及其制备方法 |
JP2018168185A (ja) * | 2018-07-05 | 2018-11-01 | 大日本住友製薬株式会社 | 溶出が良好なイルベサルタン含有医薬組成物および口腔内崩壊錠 |
PH12018000390A1 (en) * | 2018-11-20 | 2020-09-28 | Novex Science Pte Ltd | Carbocysteine and zinc tablet |
JP2019203031A (ja) * | 2019-09-06 | 2019-11-28 | 大日本住友製薬株式会社 | 溶出が良好なイルベサルタン含有医薬組成物および口腔内崩壊錠 |
GR1010320B (el) * | 2021-08-04 | 2022-10-11 | Win Medica Φαρμακευτικη Ανωνυμη Εταιρεια, | Στερεες φαρμακοτεχνικες μορφες ιρβεσαρτανης, υδροχλωροθειαζιδης και αμλοδιπινης |
Family Cites Families (12)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE3744317C1 (de) | 1987-12-28 | 1989-05-24 | Rudolf Dr Rer Nat Kuerner | Verwendung von Calciumsulfat zur Verbesserung der Fermentierung organischer Abfallstoffe |
EP0400835A1 (en) | 1989-05-15 | 1990-12-05 | Merck & Co. Inc. | Substituted benzimidazoles as angiotensin II antagonists |
US5164407A (en) | 1989-07-03 | 1992-11-17 | Merck & Co., Inc. | Substituted imidazo-fused 5-membered ring heterocycles and their use as angiotensin ii antagonsists |
IE910913A1 (en) * | 1990-03-20 | 1991-09-25 | Sanofi Sa | N-substituted heterocyclic derivates, their preparation¹and pharmaceutical compositions containing them |
US5270317A (en) * | 1990-03-20 | 1993-12-14 | Elf Sanofi | N-substituted heterocyclic derivatives, their preparation and the pharmaceutical compositions in which they are present |
IL99372A0 (en) * | 1990-09-10 | 1992-08-18 | Ciba Geigy Ag | Azacyclic compounds |
FI112942B3 (fi) | 1991-02-21 | 2012-03-13 | Daiichi Sankyo Co Ltd | Menetelmä kohonneen verenpaineen hoitoon ja ennaltaehkäisyyn käyttökelpoisten 4'-(1H-imidatsol-1-yylimetyyli)-1,1' -bifenyylijohdannaisten valmistamiseksi |
EP0502575A1 (en) | 1991-03-06 | 1992-09-09 | Merck & Co. Inc. | Substituted 1-(2H)-isoquinolinones |
WO1994009778A1 (en) * | 1992-10-26 | 1994-05-11 | Merck & Co., Inc. | Combinations of angiotensin-ii receptor antagonists and diuretics |
EP0629408A1 (en) * | 1993-06-16 | 1994-12-21 | LABORATOIRES MERCK, SHARP & DOHME-CHIBRET | Combination of angiotensin converting enzyme inhibitors and AII antagonists |
US5541209A (en) * | 1994-08-22 | 1996-07-30 | Bristol-Myers Squibb Company | Method of treating or preventing cardiac arrhythmia employing an N-substituted heterocyclic derivative |
FR2725987B1 (fr) * | 1994-10-19 | 1997-01-10 | Sanofi Sa | Procede pour la preparation d'un derive de tetrazole sous deux formes cristallines et nouvelle forme cristalline de ce derive |
-
1996
- 1996-05-16 TW TW085105820A patent/TW442301B/zh not_active IP Right Cessation
- 1996-05-17 NZ NZ286612A patent/NZ286612A/en not_active IP Right Cessation
- 1996-05-17 IL IL11830996A patent/IL118309A/xx not_active IP Right Cessation
- 1996-05-17 NZ NZ329547A patent/NZ329547A/en not_active IP Right Cessation
- 1996-05-27 SG SG1996009899A patent/SG49956A1/en unknown
- 1996-05-28 ZA ZA9604337A patent/ZA964337B/xx unknown
- 1996-05-30 CA CA002177772A patent/CA2177772C/en not_active Expired - Fee Related
- 1996-06-05 KR KR1019960019949A patent/KR100442719B1/ko not_active IP Right Cessation
- 1996-06-05 CZ CZ19961634A patent/CZ291532B6/cs not_active IP Right Cessation
- 1996-06-06 AR AR10297996A patent/AR002350A1/es not_active Application Discontinuation
- 1996-06-06 HU HU9601564A patent/HU229369B1/hu not_active IP Right Cessation
- 1996-06-06 RU RU96111030/14A patent/RU2181590C2/ru active
- 1996-06-06 AU AU54763/96A patent/AU702651B2/en not_active Ceased
- 1996-06-06 RU RU2001130903/14A patent/RU2210368C1/ru active
- 1996-06-06 NO NO19962387A patent/NO310495B1/no not_active IP Right Cessation
- 1996-06-07 ES ES02016237T patent/ES2363127T3/es not_active Expired - Lifetime
- 1996-06-07 DE DE69629755T patent/DE69629755T3/de not_active Expired - Lifetime
- 1996-06-07 DE DE69638348T patent/DE69638348D1/de not_active Expired - Lifetime
- 1996-06-07 AT AT02016237T patent/ATE503478T1/de active
- 1996-06-07 EP EP96304291A patent/EP0747050B2/en not_active Expired - Lifetime
- 1996-06-07 AT AT96304291T patent/ATE248594T1/de active
- 1996-06-07 PL PL96314670A patent/PL184893B1/pl unknown
- 1996-06-07 DK DK02016237.6T patent/DK1275391T3/da active
- 1996-06-07 EP EP02016237A patent/EP1275391B1/en not_active Expired - Lifetime
- 1996-06-07 JP JP14557996A patent/JP3162626B2/ja not_active Expired - Lifetime
- 1996-06-07 CN CNB961068329A patent/CN1149083C/zh not_active Expired - Lifetime
- 1996-06-07 PT PT02016237T patent/PT1275391E/pt unknown
- 1996-06-07 ES ES96304291T patent/ES2205000T5/es not_active Expired - Lifetime
- 1996-06-07 DK DK96304291.6T patent/DK0747050T4/da active
- 1996-06-07 PT PT96304291T patent/PT747050E/pt unknown
-
1998
- 1998-01-27 HK HK98100693A patent/HK1002384A1/xx not_active IP Right Cessation
-
2000
- 2000-09-22 NO NO20004743A patent/NO310393B1/no not_active IP Right Cessation
-
2006
- 2006-06-16 AR ARP060102579A patent/AR054782A2/es not_active Application Discontinuation
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