PE20050414A1 - Formulacion farmaceutica oral que comprende un antagonista de la bomba de protones y un excipiente basico - Google Patents
Formulacion farmaceutica oral que comprende un antagonista de la bomba de protones y un excipiente basicoInfo
- Publication number
- PE20050414A1 PE20050414A1 PE2004000357A PE2004000357A PE20050414A1 PE 20050414 A1 PE20050414 A1 PE 20050414A1 PE 2004000357 A PE2004000357 A PE 2004000357A PE 2004000357 A PE2004000357 A PE 2004000357A PE 20050414 A1 PE20050414 A1 PE 20050414A1
- Authority
- PE
- Peru
- Prior art keywords
- flavors
- capsules
- granules
- dimethyl
- pharmaceutical formulation
- Prior art date
Links
- 239000005557 antagonist Substances 0.000 title abstract 2
- 239000000546 pharmaceutical excipient Substances 0.000 title abstract 2
- 239000008203 oral pharmaceutical composition Substances 0.000 title 1
- 239000003795 chemical substances by application Substances 0.000 abstract 3
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 abstract 2
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 abstract 2
- 239000002775 capsule Substances 0.000 abstract 2
- 239000000796 flavoring agent Substances 0.000 abstract 2
- 235000019634 flavors Nutrition 0.000 abstract 2
- 239000008187 granular material Substances 0.000 abstract 2
- PWILYDZRJORZDR-MISYRCLQSA-N (7r,8r,9r)-7-(2-methoxyethoxy)-2,3-dimethyl-9-phenyl-7,8,9,10-tetrahydroimidazo[1,2-h][1,7]naphthyridin-8-ol Chemical compound C1([C@@H]2[C@@H](O)[C@@H](C3=C(C4=NC(C)=C(C)N4C=C3)N2)OCCOC)=CC=CC=C1 PWILYDZRJORZDR-MISYRCLQSA-N 0.000 abstract 1
- NQPWMHCSZYMRMV-UHFFFAOYSA-N 3-[[1-(4-methoxy-2-methylphenyl)-6-methyl-2,3-dihydropyrrolo[3,2-c]quinolin-4-yl]amino]propan-1-ol Chemical compound CC1=CC(OC)=CC=C1N1C(C=2C(=C(C)C=CC=2)N=C2NCCCO)=C2CC1 NQPWMHCSZYMRMV-UHFFFAOYSA-N 0.000 abstract 1
- 102000006270 Proton Pumps Human genes 0.000 abstract 1
- 108010083204 Proton Pumps Proteins 0.000 abstract 1
- 239000004480 active ingredient Substances 0.000 abstract 1
- 239000013543 active substance Substances 0.000 abstract 1
- 125000002737 ampicillanyl group Chemical group N[C@@H](C(=O)N[C@H]1[C@@H]2N([C@H](C(S2)(C)C)C(=O)*)C1=O)C1=CC=CC=C1 0.000 abstract 1
- 229910000019 calcium carbonate Inorganic materials 0.000 abstract 1
- 239000003086 colorant Substances 0.000 abstract 1
- 150000001875 compounds Chemical class 0.000 abstract 1
- 239000012729 immediate-release (IR) formulation Substances 0.000 abstract 1
- 239000000314 lubricant Substances 0.000 abstract 1
- ZLNQQNXFFQJAID-UHFFFAOYSA-L magnesium carbonate Chemical compound [Mg+2].[O-]C([O-])=O ZLNQQNXFFQJAID-UHFFFAOYSA-L 0.000 abstract 1
- 239000001095 magnesium carbonate Substances 0.000 abstract 1
- 229910000021 magnesium carbonate Inorganic materials 0.000 abstract 1
- VTHJTEIRLNZDEV-UHFFFAOYSA-L magnesium dihydroxide Chemical compound [OH-].[OH-].[Mg+2] VTHJTEIRLNZDEV-UHFFFAOYSA-L 0.000 abstract 1
- 239000000347 magnesium hydroxide Substances 0.000 abstract 1
- 229910001862 magnesium hydroxide Inorganic materials 0.000 abstract 1
- 239000000395 magnesium oxide Substances 0.000 abstract 1
- CPLXHLVBOLITMK-UHFFFAOYSA-N magnesium oxide Inorganic materials [Mg]=O CPLXHLVBOLITMK-UHFFFAOYSA-N 0.000 abstract 1
- AXZKOIWUVFPNLO-UHFFFAOYSA-N magnesium;oxygen(2-) Chemical compound [O-2].[Mg+2] AXZKOIWUVFPNLO-UHFFFAOYSA-N 0.000 abstract 1
- 239000000463 material Substances 0.000 abstract 1
- 239000006186 oral dosage form Substances 0.000 abstract 1
- IBBMAWULFFBRKK-UHFFFAOYSA-N picolinamide Chemical compound NC(=O)C1=CC=CC=N1 IBBMAWULFFBRKK-UHFFFAOYSA-N 0.000 abstract 1
- 229910000029 sodium carbonate Inorganic materials 0.000 abstract 1
- 229950004825 soraprazan Drugs 0.000 abstract 1
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
-
- 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
- A61K31/00—Medicinal preparations containing organic active ingredients
-
- 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
- A61K31/4353—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 ortho- or peri-condensed with heterocyclic ring systems
- A61K31/4375—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 ortho- or peri-condensed with heterocyclic ring systems the heterocyclic ring system containing a six-membered ring having nitrogen as a ring heteroatom, e.g. quinolizines, naphthyridines, berberine, vincamine
-
- 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
- A61K31/4427—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
- A61K31/4439—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems containing a five-membered ring with nitrogen as a ring hetero atom, e.g. omeprazole
-
- 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
-
- 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
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- 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
- A61K9/28—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
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Epidemiology (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Organic Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Inorganic Chemistry (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Medicinal Preparation (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
Abstract
SE REFIERE A UNA FORMA DE DOSIFICACION POR VIA ORAL, ESTABLES, PARA AGENTES ANTAGONISTAS DE BOMBAS DE PROTONES (APAs), SIENDO SELECCIONADOS LOS COMPUESTOS: AU-461, 7R,8R,9R)-2,3-DIMETIL-8-HIDROXI-7-(2-METOXIETOXI)-9-FENIL-7,8,9,10-TETRAHIDROIMIDAZO[1,2-h][1,7]NAFTIRIDINA (INN SORAPRAZANO), DBM-819, KR-60436, T-330, YH-1885, YJA-20379-8 Y 2,3-DIMETIL-8-(2-ETIL-6-METILBENCILAMINO)IMIDAZOL[1,2-a]PIRIDINA-6-CARBOXAMIDA, EN EL CUAL ESTE AGENTE ES ESTABILIZADO MEDIANTE UN EXCIPIENTE DE CARACTER BASICO TALES COMO CARBONATO DE SODIO, CARBONATO DE CALCIO, CARBONATO DE MAGNESIO, OXIDO DE MAGNESIO, HIDROXIDO DE MAGNESIO, ENTRE OTROS, LOS QUE ESTAN PRESENTES EN FORMA FINAMENTE DIVIDIDA Y MEZCLADOS A FONDO CON EL AGENTE, OBTENIENDOSE UNA FORMA DE DOSIFICACION QUE SE DESINTEGRA CON RAPIDEZ CON UNA LIBERACION INMEDIATA DEL INGREDIENTE ACTIVO, ADEMAS PRESENTAN POR LO MENOS UN MATERIAL DE RELLENO Y UN AGENTE DESINTEGRANTE, Y UNO O MAS EXCIPENTES ADICIONALES COMO LUBRICANTES, AROMATIZANTES, COLORANTES, SABOREANTES Y SUSTANCIAS ACTIVAS SUPERFICIALMENTE. LAS FORMA DE DOSIFICACION ORAL SE SELECCIONA ENTRE TABLETAS, TABLETAS REVESTIDAS, GRANULOS, MICROTABLETAS EN CAPSULAS Y GRANULOS EN CAPSULAS
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE10317023A DE10317023A1 (de) | 2003-04-11 | 2003-04-11 | Perorale Arzneimittelzubereitung für Protonenpumpenantagonisten |
| EP03008453 | 2003-04-11 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| PE20050414A1 true PE20050414A1 (es) | 2005-06-18 |
Family
ID=33160619
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PE2004000357A PE20050414A1 (es) | 2003-04-11 | 2004-04-07 | Formulacion farmaceutica oral que comprende un antagonista de la bomba de protones y un excipiente basico |
Country Status (19)
| Country | Link |
|---|---|
| US (1) | US20060204568A1 (es) |
| EP (1) | EP1615624A2 (es) |
| JP (1) | JP2006522776A (es) |
| KR (1) | KR20060002932A (es) |
| AR (1) | AR044004A1 (es) |
| AU (1) | AU2004228961A1 (es) |
| BR (1) | BRPI0409175A (es) |
| CA (1) | CA2526869A1 (es) |
| CL (1) | CL2004000767A1 (es) |
| EA (1) | EA200501565A1 (es) |
| IS (1) | IS8107A (es) |
| MA (1) | MA27772A1 (es) |
| MX (1) | MXPA05010705A (es) |
| NO (1) | NO20055207L (es) |
| PE (1) | PE20050414A1 (es) |
| RS (1) | RS20050756A (es) |
| TN (1) | TNSN05233A1 (es) |
| TW (1) | TW200503783A (es) |
| WO (1) | WO2004089342A2 (es) |
Families Citing this family (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| PE20050150A1 (es) * | 2003-05-08 | 2005-03-22 | Altana Pharma Ag | Una forma de dosificacion que contiene (s)-pantoprazol como ingrediente activo |
| EP1799211A1 (en) * | 2004-10-05 | 2007-06-27 | Altana Pharma AG | Oral pharmaceutical preparation comprising a proton pump antagonist and a basic excipient |
| US20100047338A1 (en) | 2008-03-14 | 2010-02-25 | Angela Brodie | Novel C-17-Heteroaryl Steroidal CYP17 Inhibitors/Antiandrogens, In Vitro Biological Activities, Pharmacokinetics and Antitumor Activity |
| US20080194307A1 (en) * | 2007-02-13 | 2008-08-14 | Jeff Sanger | Sports-based game of chance |
| MY159358A (en) | 2007-10-12 | 2016-12-30 | Novartis Ag | Compositions comprising sphingosine 1 phosphate (s1p) receptor modulators |
| CN102743330B (zh) | 2008-07-28 | 2016-03-23 | 武田药品工业株式会社 | 药物组合物 |
| EP3288556A4 (en) | 2015-04-29 | 2018-09-19 | Dexcel Pharma Technologies Ltd. | Orally disintegrating compositions |
| CR20180119A (es) | 2015-07-30 | 2018-03-21 | Takeda Pharmaceuticals Co | Tableta |
| US10076494B2 (en) | 2016-06-16 | 2018-09-18 | Dexcel Pharma Technologies Ltd. | Stable orally disintegrating pharmaceutical compositions |
Family Cites Families (17)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4464372A (en) * | 1982-08-16 | 1984-08-07 | Schering Corporation | Imidazo[1,2-b]pyridazines |
| GB8422461D0 (en) * | 1984-09-05 | 1984-10-10 | Wyeth John & Brother Ltd | Pyridine derivatives |
| GB2189698A (en) * | 1986-04-30 | 1987-11-04 | Haessle Ab | Coated omeprazole tablets |
| US4833149A (en) * | 1986-09-22 | 1989-05-23 | Ortho Pharmaceutical Corporation | 2- or 3-aryl substituted imidazo[1,2-a]pyridines |
| US5041442A (en) * | 1990-07-31 | 1991-08-20 | Syntex (U.S.A.) Inc. | Pyrrolo(1,2-a)pyrazines as inhibitors of gastric acid secretion |
| US5362743A (en) * | 1993-03-09 | 1994-11-08 | Pfizer Inc. | Aminoquinoline derivatives |
| US6645988B2 (en) * | 1996-01-04 | 2003-11-11 | Curators Of The University Of Missouri | Substituted benzimidazole dosage forms and method of using same |
| EA002402B1 (ru) * | 1997-03-24 | 2002-04-25 | Бык Гульден Ломберг Хемише Фабрик Гмбх | Тетрагидропиридо-соединения |
| AU7375598A (en) * | 1997-05-09 | 1998-11-27 | Sage Pharmaceuticals, Inc. | Stable oral pharmaceutical dosage forms |
| TW580397B (en) * | 1997-05-27 | 2004-03-21 | Takeda Chemical Industries Ltd | Solid preparation |
| SK285165B6 (sk) * | 1998-09-23 | 2006-07-07 | Altana Pharma Ag | Tetrahydropyridoétery, farmaceutický prostriedok s ich obsahom a ich použitie |
| DE19925710C2 (de) * | 1999-06-07 | 2002-10-10 | Byk Gulden Lomberg Chem Fab | Neue Zubereitung und Darreichungsform enthaltend einen säurelabilen Protonenpumpenhemmer |
| UA74339C2 (uk) * | 1999-06-07 | 2005-12-15 | Алтана Фарма Аг | Форма для введення, що включає інгібітор протонної помпи у вигляді окремих одиниць, та спосіб їх одержання |
| IL130602A0 (en) * | 1999-06-22 | 2000-06-01 | Dexcel Ltd | Stable benzimidazole formulation |
| WO2001028559A1 (en) * | 1999-10-20 | 2001-04-26 | Eisai Co., Ltd. | Method for stabilizing benzimidazole compounds |
| UA80393C2 (uk) * | 2000-12-07 | 2007-09-25 | Алтана Фарма Аг | Фармацевтична композиція, яка містить інгібітор фде 4, диспергований в матриці |
| US20040028737A1 (en) * | 2002-08-12 | 2004-02-12 | Kopran Research Laboratories Limited | Enteric coated stable oral pharmaceutical composition of acid unstable drug and process for preparing the same |
-
2004
- 2004-04-01 TW TW093109111A patent/TW200503783A/zh unknown
- 2004-04-07 AR ARP040101186A patent/AR044004A1/es not_active Application Discontinuation
- 2004-04-07 PE PE2004000357A patent/PE20050414A1/es not_active Application Discontinuation
- 2004-04-08 CA CA002526869A patent/CA2526869A1/en not_active Abandoned
- 2004-04-08 MX MXPA05010705A patent/MXPA05010705A/es unknown
- 2004-04-08 WO PCT/EP2004/050493 patent/WO2004089342A2/en not_active Ceased
- 2004-04-08 AU AU2004228961A patent/AU2004228961A1/en not_active Abandoned
- 2004-04-08 BR BRPI0409175-2A patent/BRPI0409175A/pt not_active IP Right Cessation
- 2004-04-08 RS YUP-2005/0756A patent/RS20050756A/sr unknown
- 2004-04-08 KR KR1020057018865A patent/KR20060002932A/ko not_active Withdrawn
- 2004-04-08 US US10/551,943 patent/US20060204568A1/en not_active Abandoned
- 2004-04-08 EA EA200501565A patent/EA200501565A1/ru unknown
- 2004-04-08 EP EP04726521A patent/EP1615624A2/en not_active Withdrawn
- 2004-04-08 JP JP2006505541A patent/JP2006522776A/ja not_active Withdrawn
- 2004-04-08 CL CL200400767A patent/CL2004000767A1/es unknown
-
2005
- 2005-09-23 TN TNP2005000233A patent/TNSN05233A1/en unknown
- 2005-10-31 IS IS8107A patent/IS8107A/is unknown
- 2005-11-02 MA MA28575A patent/MA27772A1/fr unknown
- 2005-11-04 NO NO20055207A patent/NO20055207L/no not_active Application Discontinuation
Also Published As
| Publication number | Publication date |
|---|---|
| MA27772A1 (fr) | 2006-02-01 |
| CA2526869A1 (en) | 2004-10-21 |
| WO2004089342A2 (en) | 2004-10-21 |
| JP2006522776A (ja) | 2006-10-05 |
| IS8107A (is) | 2005-10-31 |
| CL2004000767A1 (es) | 2005-05-27 |
| NO20055207L (no) | 2005-11-04 |
| TNSN05233A1 (en) | 2007-06-11 |
| BRPI0409175A (pt) | 2006-04-11 |
| US20060204568A1 (en) | 2006-09-14 |
| MXPA05010705A (es) | 2005-12-12 |
| TW200503783A (en) | 2005-02-01 |
| RS20050756A (sr) | 2007-11-15 |
| KR20060002932A (ko) | 2006-01-09 |
| WO2004089342A3 (en) | 2005-03-10 |
| EP1615624A2 (en) | 2006-01-18 |
| AU2004228961A1 (en) | 2004-10-21 |
| AR044004A1 (es) | 2005-08-24 |
| EA200501565A1 (ru) | 2006-06-30 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| FX | Voluntary withdrawal |