SK12092002A3 - Formulácie tabliet obsahujúce oxazolidinóny - Google Patents
Formulácie tabliet obsahujúce oxazolidinóny Download PDFInfo
- Publication number
- SK12092002A3 SK12092002A3 SK1209-2002A SK12092002A SK12092002A3 SK 12092002 A3 SK12092002 A3 SK 12092002A3 SK 12092002 A SK12092002 A SK 12092002A SK 12092002 A3 SK12092002 A3 SK 12092002A3
- Authority
- SK
- Slovakia
- Prior art keywords
- starch
- linezolid
- microcrystalline cellulose
- hydroxymethyl
- hydroxypropyl
- Prior art date
Links
- IZXIZTKNFFYFOF-UHFFFAOYSA-N 2-Oxazolidone Chemical compound O=C1NCCO1 IZXIZTKNFFYFOF-UHFFFAOYSA-N 0.000 title claims abstract description 28
- 239000007916 tablet composition Substances 0.000 title description 6
- 239000007891 compressed tablet Substances 0.000 claims abstract description 34
- 230000000844 anti-bacterial effect Effects 0.000 claims abstract description 24
- HQKMJHAJHXVSDF-UHFFFAOYSA-L magnesium stearate Chemical group [Mg+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O HQKMJHAJHXVSDF-UHFFFAOYSA-L 0.000 claims description 63
- TYZROVQLWOKYKF-ZDUSSCGKSA-N linezolid Chemical compound O=C1O[C@@H](CNC(=O)C)CN1C(C=C1F)=CC=C1N1CCOCC1 TYZROVQLWOKYKF-ZDUSSCGKSA-N 0.000 claims description 57
- 229960003907 linezolid Drugs 0.000 claims description 55
- 229920000168 Microcrystalline cellulose Polymers 0.000 claims description 48
- 229940016286 microcrystalline cellulose Drugs 0.000 claims description 48
- 239000008108 microcrystalline cellulose Substances 0.000 claims description 48
- 235000019813 microcrystalline cellulose Nutrition 0.000 claims description 47
- 239000003826 tablet Substances 0.000 claims description 40
- 229920002153 Hydroxypropyl cellulose Polymers 0.000 claims description 39
- 239000001863 hydroxypropyl cellulose Substances 0.000 claims description 39
- 235000010977 hydroxypropyl cellulose Nutrition 0.000 claims description 39
- 229920002261 Corn starch Polymers 0.000 claims description 36
- 239000000203 mixture Substances 0.000 claims description 34
- 125000004029 hydroxymethyl group Chemical group [H]OC([H])([H])* 0.000 claims description 31
- 235000019359 magnesium stearate Nutrition 0.000 claims description 31
- 239000011230 binding agent Substances 0.000 claims description 24
- 238000000034 method Methods 0.000 claims description 24
- 229920002472 Starch Polymers 0.000 claims description 23
- 229940080313 sodium starch Drugs 0.000 claims description 23
- 229940032147 starch Drugs 0.000 claims description 23
- 239000008107 starch Substances 0.000 claims description 23
- 235000019698 starch Nutrition 0.000 claims description 23
- 235000019759 Maize starch Nutrition 0.000 claims description 21
- -1 hydroxypropyl Chemical group 0.000 claims description 19
- 239000008120 corn starch Substances 0.000 claims description 15
- 229920002785 Croscarmellose sodium Polymers 0.000 claims description 12
- 235000021355 Stearic acid Nutrition 0.000 claims description 10
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 claims description 10
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 claims description 10
- 239000008117 stearic acid Substances 0.000 claims description 10
- DLFVBJFMPXGRIB-UHFFFAOYSA-N Acetamide Chemical compound CC(N)=O DLFVBJFMPXGRIB-UHFFFAOYSA-N 0.000 claims description 9
- 239000011734 sodium Substances 0.000 claims description 9
- 229910052708 sodium Inorganic materials 0.000 claims description 9
- WHNWPMSKXPGLAX-UHFFFAOYSA-N N-Vinyl-2-pyrrolidone Chemical compound C=CN1CCCC1=O WHNWPMSKXPGLAX-UHFFFAOYSA-N 0.000 claims description 8
- 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 8
- 229960001681 croscarmellose sodium Drugs 0.000 claims description 8
- 235000010947 crosslinked sodium carboxy methyl cellulose Nutrition 0.000 claims description 8
- 239000007884 disintegrant Substances 0.000 claims description 8
- 239000013078 crystal Substances 0.000 claims description 7
- 239000000314 lubricant Substances 0.000 claims description 7
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 claims description 6
- 230000036765 blood level Effects 0.000 claims description 6
- 239000001866 hydroxypropyl methyl cellulose Substances 0.000 claims description 6
- 235000010979 hydroxypropyl methyl cellulose Nutrition 0.000 claims description 6
- 229920003088 hydroxypropyl methyl cellulose Polymers 0.000 claims description 6
- UFVKGYZPFZQRLF-UHFFFAOYSA-N hydroxypropyl methyl cellulose Chemical compound OC1C(O)C(OC)OC(CO)C1OC1C(O)C(O)C(OC2C(C(O)C(OC3C(C(O)C(O)C(CO)O3)O)C(CO)O2)O)C(CO)O1 UFVKGYZPFZQRLF-UHFFFAOYSA-N 0.000 claims description 6
- 229910052751 metal Inorganic materials 0.000 claims description 6
- 239000002184 metal Substances 0.000 claims description 6
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 6
- 229920000036 polyvinylpyrrolidone Polymers 0.000 claims description 6
- 235000013855 polyvinylpyrrolidone Nutrition 0.000 claims description 6
- 229940069328 povidone Drugs 0.000 claims description 6
- 239000000454 talc Substances 0.000 claims description 6
- 229910052623 talc Inorganic materials 0.000 claims description 6
- 235000015112 vegetable and seed oil Nutrition 0.000 claims description 6
- 239000008158 vegetable oil Substances 0.000 claims description 6
- 229950008631 eperezolid Drugs 0.000 claims description 5
- 238000001990 intravenous administration Methods 0.000 claims description 5
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 5
- SIMWTRCFFSTNMG-AWEZNQCLSA-N n-[[(5s)-3-[3-fluoro-4-[4-(2-hydroxyacetyl)piperazin-1-yl]phenyl]-2-oxo-1,3-oxazolidin-5-yl]methyl]acetamide Chemical compound O=C1O[C@@H](CNC(=O)C)CN1C(C=C1F)=CC=C1N1CCN(C(=O)CO)CC1 SIMWTRCFFSTNMG-AWEZNQCLSA-N 0.000 claims description 5
- 150000003839 salts Chemical class 0.000 claims description 5
- 239000011436 cob Substances 0.000 claims description 4
- 159000000000 sodium salts Chemical class 0.000 claims description 4
- 229960000913 crospovidone Drugs 0.000 claims description 2
- 229920000523 polyvinylpolypyrrolidone Polymers 0.000 claims description 2
- 235000013809 polyvinylpolypyrrolidone Nutrition 0.000 claims description 2
- 229940031703 low substituted hydroxypropyl cellulose Drugs 0.000 claims 1
- 239000003795 chemical substances by application Substances 0.000 abstract 1
- 239000003814 drug Substances 0.000 abstract 1
- 229940079593 drug Drugs 0.000 abstract 1
- 239000011248 coating agent Substances 0.000 description 17
- 238000000576 coating method Methods 0.000 description 17
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 15
- 238000009472 formulation Methods 0.000 description 13
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 13
- 239000008187 granular material Substances 0.000 description 11
- 239000002904 solvent Substances 0.000 description 11
- 238000002156 mixing Methods 0.000 description 10
- 239000000725 suspension Substances 0.000 description 10
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 9
- 239000008213 purified water Substances 0.000 description 8
- 238000003756 stirring Methods 0.000 description 8
- 239000004615 ingredient Substances 0.000 description 7
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 6
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 6
- 239000007787 solid Substances 0.000 description 6
- 238000005469 granulation Methods 0.000 description 5
- 230000003179 granulation Effects 0.000 description 5
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 4
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 4
- VJHCJDRQFCCTHL-UHFFFAOYSA-N acetic acid 2,3,4,5,6-pentahydroxyhexanal Chemical compound CC(O)=O.OCC(O)C(O)C(O)C(O)C=O VJHCJDRQFCCTHL-UHFFFAOYSA-N 0.000 description 4
- 239000003242 anti bacterial agent Substances 0.000 description 4
- 229960005168 croscarmellose Drugs 0.000 description 4
- 239000001767 crosslinked sodium carboxy methyl cellulose Substances 0.000 description 4
- 238000001033 granulometry Methods 0.000 description 4
- 239000012071 phase Substances 0.000 description 4
- 239000000843 powder Substances 0.000 description 4
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 3
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 3
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 150000001875 compounds Chemical class 0.000 description 3
- 238000002360 preparation method Methods 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- BZLVMXJERCGZMT-UHFFFAOYSA-N Methyl tert-butyl ether Chemical compound COC(C)(C)C BZLVMXJERCGZMT-UHFFFAOYSA-N 0.000 description 2
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 2
- 239000013543 active substance Substances 0.000 description 2
- 238000007906 compression Methods 0.000 description 2
- 230000006835 compression Effects 0.000 description 2
- 238000002425 crystallisation Methods 0.000 description 2
- 230000008025 crystallization Effects 0.000 description 2
- 238000009792 diffusion process Methods 0.000 description 2
- 238000004090 dissolution Methods 0.000 description 2
- 229940071676 hydroxypropylcellulose Drugs 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- IAQNDIYXOKAHJQ-AWEZNQCLSA-N n-[[(5s)-3-[3-fluoro-4-(thian-4-yl)phenyl]-2-oxo-1,3-oxazolidin-5-yl]methyl]acetamide Chemical compound O=C1O[C@@H](CNC(=O)C)CN1C(C=C1F)=CC=C1C1CCSCC1 IAQNDIYXOKAHJQ-AWEZNQCLSA-N 0.000 description 2
- 238000005498 polishing Methods 0.000 description 2
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 2
- 230000001012 protector Effects 0.000 description 2
- 238000007873 sieving Methods 0.000 description 2
- 239000007790 solid phase Substances 0.000 description 2
- 239000007921 spray Substances 0.000 description 2
- 238000009492 tablet coating Methods 0.000 description 2
- 239000002700 tablet coating Substances 0.000 description 2
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 description 1
- 241000192125 Firmicutes Species 0.000 description 1
- GUBGYTABKSRVRQ-QKKXKWKRSA-N Lactose Natural products OC[C@H]1O[C@@H](O[C@H]2[C@H](O)[C@@H](O)C(O)O[C@@H]2CO)[C@H](O)[C@@H](O)[C@H]1O GUBGYTABKSRVRQ-QKKXKWKRSA-N 0.000 description 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 239000003153 chemical reaction reagent Substances 0.000 description 1
- 239000008199 coating composition Substances 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 238000004821 distillation Methods 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 239000012530 fluid Substances 0.000 description 1
- 239000004519 grease Substances 0.000 description 1
- 229920003063 hydroxymethyl cellulose Polymers 0.000 description 1
- 229940031574 hydroxymethyl cellulose Drugs 0.000 description 1
- 238000002372 labelling Methods 0.000 description 1
- 239000008101 lactose Substances 0.000 description 1
- 239000002480 mineral oil Substances 0.000 description 1
- 235000010446 mineral oil Nutrition 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 230000000144 pharmacologic effect Effects 0.000 description 1
- RYYKJJJTJZKILX-UHFFFAOYSA-M sodium octadecanoate Chemical group [Na+].CCCCCCCCCCCCCCCCCC([O-])=O RYYKJJJTJZKILX-UHFFFAOYSA-M 0.000 description 1
- 239000011877 solvent mixture Substances 0.000 description 1
- 238000001228 spectrum Methods 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 230000002110 toxicologic effect Effects 0.000 description 1
- 231100000027 toxicology Toxicity 0.000 description 1
- 239000008096 xylene Substances 0.000 description 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
- A61K9/2022—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
- 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
- A61K31/42—Oxazoles
- A61K31/422—Oxazoles not condensed and containing further heterocyclic rings
-
- 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
- A61K31/496—Non-condensed piperazines containing further heterocyclic rings, e.g. rifampin, thiothixene or sparfloxacin
-
- 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
- A61K31/535—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 oxygen as the ring hetero atoms, e.g. 1,2-oxazines
- A61K31/5375—1,4-Oxazines, e.g. morpholine
- A61K31/5377—1,4-Oxazines, e.g. morpholine not condensed and containing further heterocyclic rings, e.g. timolol
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/04—Antibacterial agents
Landscapes
- Health & Medical Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Veterinary Medicine (AREA)
- Chemical & Material Sciences (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Epidemiology (AREA)
- Organic Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Oncology (AREA)
- Communicable Diseases (AREA)
- Medicinal Preparation (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Infusion, Injection, And Reservoir Apparatuses (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US19096900P | 2000-03-22 | 2000-03-22 | |
| PCT/US2001/005812 WO2001070225A2 (en) | 2000-03-22 | 2001-03-15 | Oxazolidinone tablet formulation |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| SK12092002A3 true SK12092002A3 (sk) | 2002-12-03 |
Family
ID=22703542
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| SK1209-2002A SK12092002A3 (sk) | 2000-03-22 | 2001-03-15 | Formulácie tabliet obsahujúce oxazolidinóny |
Country Status (33)
| Country | Link |
|---|---|
| EP (1) | EP1265608B1 (pl) |
| JP (1) | JP2003527424A (pl) |
| KR (2) | KR20070094673A (pl) |
| CN (1) | CN1208058C (pl) |
| AR (1) | AR033357A1 (pl) |
| AT (1) | ATE412413T1 (pl) |
| AU (2) | AU4324301A (pl) |
| BG (1) | BG107117A (pl) |
| BR (1) | BR0108846A (pl) |
| CA (1) | CA2400118A1 (pl) |
| CZ (1) | CZ20023133A3 (pl) |
| DE (1) | DE60136341D1 (pl) |
| DK (1) | DK1265608T3 (pl) |
| EA (1) | EA006772B1 (pl) |
| EC (1) | ECSP013979A (pl) |
| ES (1) | ES2312422T3 (pl) |
| HK (1) | HK1054325B (pl) |
| HR (1) | HRP20020765A2 (pl) |
| HU (1) | HUP0300378A3 (pl) |
| IL (1) | IL151788A0 (pl) |
| MX (1) | MXPA02009316A (pl) |
| MY (1) | MY136370A (pl) |
| NO (1) | NO20024505L (pl) |
| NZ (1) | NZ521525A (pl) |
| PE (2) | PE20011126A1 (pl) |
| PL (1) | PL201686B1 (pl) |
| PT (1) | PT1265608E (pl) |
| SK (1) | SK12092002A3 (pl) |
| TW (1) | TWI293028B (pl) |
| UA (1) | UA77654C2 (pl) |
| WO (1) | WO2001070225A2 (pl) |
| YU (1) | YU69802A (pl) |
| ZA (1) | ZA200207073B (pl) |
Families Citing this family (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB0209265D0 (en) | 2002-04-23 | 2002-06-05 | Novartis Ag | Organic compounds |
| ES2309920T3 (es) * | 2005-07-20 | 2008-12-16 | Teva Pharmaceutical Industries Ltd. | Composicion farmaceutica estable que comprende la forma iii de linezolid. |
| WO2010026597A1 (en) * | 2008-09-02 | 2010-03-11 | Hetero Research Foundation | Oral dosage forms of linezolid and processes for their preparation |
| ES2836809T3 (es) * | 2010-11-24 | 2021-06-28 | Melinta Subsidiary Corp | Composiciones farmacéuticas |
| WO2013088389A1 (en) * | 2011-12-14 | 2013-06-20 | Alembic Pharmaceuticals Limited | Linezolid premix |
| CN103505459B (zh) * | 2012-06-20 | 2016-02-24 | 北京万生药业有限责任公司 | 利奈唑胺药物组合物 |
| CN104622831B (zh) * | 2013-11-06 | 2018-06-22 | 江苏豪森药业集团有限公司 | 一种口服片剂及其制备方法 |
| BR112017021097B1 (pt) | 2015-04-01 | 2024-01-02 | Akebia Therapeutics, Inc | Formulação de dosagem oral e seu uso |
| CN106727396A (zh) * | 2016-11-22 | 2017-05-31 | 湖北广济药业股份有限公司 | 一种ⅱ晶型利奈唑胺片及其制备方法 |
| CN109481412A (zh) * | 2018-08-17 | 2019-03-19 | 扬子江药业集团北京海燕药业有限公司 | 一种ii晶型利奈唑胺片及其制备工艺 |
Family Cites Families (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3993767A (en) * | 1975-11-18 | 1976-11-23 | A. H. Robins Company, Incorporated | Compositions to suppress gastric bleeding in indomethacin and phenylbutazone therapy |
| AUPP437698A0 (en) * | 1998-06-30 | 1998-07-23 | Baumgart, Karl | Methods for treatment of coronary, carotid and other vascular disease |
| AU767380B2 (en) * | 1999-05-27 | 2003-11-06 | Pharmacia & Upjohn Company | Bicyclic oxazolidinones as antibacterial agent |
-
2001
- 2001-03-15 DE DE60136341T patent/DE60136341D1/de not_active Expired - Fee Related
- 2001-03-15 MX MXPA02009316A patent/MXPA02009316A/es not_active Application Discontinuation
- 2001-03-15 DK DK01916186T patent/DK1265608T3/da active
- 2001-03-15 AU AU4324301A patent/AU4324301A/xx active Pending
- 2001-03-15 EA EA200201006A patent/EA006772B1/ru not_active IP Right Cessation
- 2001-03-15 CA CA002400118A patent/CA2400118A1/en not_active Abandoned
- 2001-03-15 ES ES01916186T patent/ES2312422T3/es not_active Expired - Lifetime
- 2001-03-15 HU HU0300378A patent/HUP0300378A3/hu unknown
- 2001-03-15 IL IL15178801A patent/IL151788A0/xx unknown
- 2001-03-15 AT AT01916186T patent/ATE412413T1/de not_active IP Right Cessation
- 2001-03-15 CN CNB018064698A patent/CN1208058C/zh not_active Expired - Fee Related
- 2001-03-15 YU YU69802A patent/YU69802A/sh unknown
- 2001-03-15 UA UA2002108322A patent/UA77654C2/uk unknown
- 2001-03-15 AU AU2001243243A patent/AU2001243243B2/en not_active Ceased
- 2001-03-15 KR KR1020077020576A patent/KR20070094673A/ko not_active Application Discontinuation
- 2001-03-15 NZ NZ521525A patent/NZ521525A/en unknown
- 2001-03-15 PL PL366067A patent/PL201686B1/pl unknown
- 2001-03-15 PT PT01916186T patent/PT1265608E/pt unknown
- 2001-03-15 SK SK1209-2002A patent/SK12092002A3/sk unknown
- 2001-03-15 BR BR0108846-7A patent/BR0108846A/pt not_active IP Right Cessation
- 2001-03-15 JP JP2001568423A patent/JP2003527424A/ja not_active Ceased
- 2001-03-15 CZ CZ20023133A patent/CZ20023133A3/cs unknown
- 2001-03-15 WO PCT/US2001/005812 patent/WO2001070225A2/en active IP Right Grant
- 2001-03-15 KR KR1020027012465A patent/KR100786410B1/ko not_active IP Right Cessation
- 2001-03-15 EP EP01916186A patent/EP1265608B1/en not_active Revoked
- 2001-03-20 MY MYPI20011303A patent/MY136370A/en unknown
- 2001-03-22 PE PE2001000273A patent/PE20011126A1/es not_active Application Discontinuation
- 2001-03-22 AR ARP010101348A patent/AR033357A1/es unknown
- 2001-03-22 TW TW090106735A patent/TWI293028B/zh active
- 2001-03-22 EC EC2001003979A patent/ECSP013979A/es unknown
- 2001-05-15 PE PE2001000437U patent/PE20020499Z/es not_active IP Right Cessation
-
2002
- 2002-09-03 ZA ZA200207073A patent/ZA200207073B/en unknown
- 2002-09-18 BG BG107117A patent/BG107117A/bg unknown
- 2002-09-19 HR HR20020765A patent/HRP20020765A2/hr not_active Application Discontinuation
- 2002-09-20 NO NO20024505A patent/NO20024505L/no not_active Application Discontinuation
-
2003
- 2003-09-11 HK HK03106507.0A patent/HK1054325B/zh not_active IP Right Cessation
Also Published As
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| CN1630510B (zh) | 药物形式的阿托伐他汀钙、其组合物和包含阿托伐他汀钙的药物制剂 | |
| JP6875407B2 (ja) | Ｊａｋキナーゼ阻害剤またはその薬剤的に許容される塩を含有する医薬組成物 | |
| EP2068839B1 (en) | Pharmaceutical compositions comprising nilotinib or its salt | |
| US9370577B2 (en) | Pharmaceutical compositions comprising entacapone, levodopa, and carbidopa | |
| US6514529B2 (en) | Oxazolidinone tablet formulation | |
| CA2612481A1 (en) | Stable pharmaceutical composition comprising linezolid form iv | |
| US20070219250A1 (en) | Pharmaceutical Compositions of Nateglinide | |
| SK12092002A3 (sk) | Formulácie tabliet obsahujúce oxazolidinóny | |
| WO2009140105A2 (en) | Formulations for cathepsin k inhibitors | |
| US9132132B2 (en) | Pharmaceutical compositions of linezolid | |
| AU2001243243A1 (en) | Oxazolidinone tablet formulation | |
| WO2007102082A1 (en) | High oxazolidinone content solid dosage forms | |
| WO2010125572A1 (en) | Compressed tablets and capsules containing efavirenz | |
| KR20110092804A (ko) | 피타바스타틴 칼슘염을 함유하는 약학 조성물 | |
| WO2017125841A1 (en) | Pharmaceutical compositions of teriflunomide | |
| JP6233911B2 (ja) | 化学的な安定性が向上したイルベサルタン含有錠剤 | |
| JP2021116239A (ja) | 溶出制御されたダサチニブ無水物含有医薬組成物 | |
| TR202022612A2 (tr) | Alogli̇pti̇ni̇n farmasöti̇k kapsül kompozi̇syonlari | |
| JP2018009032A (ja) | 化学的な安定性が向上したイルベサルタン含有錠剤 |