ES2223209B1 - Nuevas formas cristalinas del meloxicam y procedimientos para su preparacion e interconversion. - Google Patents
Nuevas formas cristalinas del meloxicam y procedimientos para su preparacion e interconversion.Info
- Publication number
- ES2223209B1 ES2223209B1 ES200102743A ES200102743A ES2223209B1 ES 2223209 B1 ES2223209 B1 ES 2223209B1 ES 200102743 A ES200102743 A ES 200102743A ES 200102743 A ES200102743 A ES 200102743A ES 2223209 B1 ES2223209 B1 ES 2223209B1
- Authority
- ES
- Spain
- Prior art keywords
- meloxicam
- temperature
- water
- preparation
- crystal
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Fee Related
Links
- ZRVUJXDFFKFLMG-UHFFFAOYSA-N Meloxicam Chemical compound OC=1C2=CC=CC=C2S(=O)(=O)N(C)C=1C(=O)NC1=NC=C(C)S1 ZRVUJXDFFKFLMG-UHFFFAOYSA-N 0.000 title claims abstract description 158
- 229960001929 meloxicam Drugs 0.000 title claims abstract description 142
- 238000000034 method Methods 0.000 title claims abstract description 71
- 238000002360 preparation method Methods 0.000 title claims abstract description 48
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 claims description 102
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 79
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 claims description 59
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 claims description 42
- 238000010992 reflux Methods 0.000 claims description 39
- 239000000203 mixture Substances 0.000 claims description 35
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 30
- 239000002244 precipitate Substances 0.000 claims description 27
- 239000000725 suspension Substances 0.000 claims description 24
- 239000002253 acid Substances 0.000 claims description 22
- 239000013078 crystal Substances 0.000 claims description 20
- 238000006243 chemical reaction Methods 0.000 claims description 19
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 claims description 16
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 claims description 15
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 claims description 14
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 claims description 14
- 239000003960 organic solvent Substances 0.000 claims description 14
- 239000008096 xylene Substances 0.000 claims description 14
- 238000003756 stirring Methods 0.000 claims description 9
- 238000001228 spectrum Methods 0.000 claims description 8
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical group C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 claims description 6
- 238000001069 Raman spectroscopy Methods 0.000 claims description 5
- 238000004090 dissolution Methods 0.000 claims description 4
- 238000002329 infrared spectrum Methods 0.000 claims description 4
- IYWCBYFJFZCCGV-UHFFFAOYSA-N formamide;hydrate Chemical compound O.NC=O IYWCBYFJFZCCGV-UHFFFAOYSA-N 0.000 claims description 3
- 238000001556 precipitation Methods 0.000 claims description 3
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 claims description 3
- 230000002378 acidificating effect Effects 0.000 claims description 2
- 125000003944 tolyl group Chemical group 0.000 claims 1
- 239000000047 product Substances 0.000 description 16
- 239000011521 glass Substances 0.000 description 13
- 239000004809 Teflon Substances 0.000 description 11
- 229920006362 Teflon® Polymers 0.000 description 11
- 239000002826 coolant Substances 0.000 description 9
- 239000003507 refrigerant Substances 0.000 description 9
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 8
- AFVFQIVMOAPDHO-UHFFFAOYSA-N Methanesulfonic acid Chemical compound CS(O)(=O)=O AFVFQIVMOAPDHO-UHFFFAOYSA-N 0.000 description 8
- 238000013019 agitation Methods 0.000 description 8
- 230000009466 transformation Effects 0.000 description 8
- 238000003760 magnetic stirring Methods 0.000 description 6
- 238000002425 crystallisation Methods 0.000 description 5
- 230000008025 crystallization Effects 0.000 description 5
- 102100038277 Prostaglandin G/H synthase 1 Human genes 0.000 description 4
- 108050003243 Prostaglandin G/H synthase 1 Proteins 0.000 description 4
- 102100038280 Prostaglandin G/H synthase 2 Human genes 0.000 description 4
- 108050003267 Prostaglandin G/H synthase 2 Proteins 0.000 description 4
- 150000001875 compounds Chemical class 0.000 description 4
- 229940098779 methanesulfonic acid Drugs 0.000 description 4
- RFFLAFLAYFXFSW-UHFFFAOYSA-N 1,2-dichlorobenzene Chemical compound ClC1=CC=CC=C1Cl RFFLAFLAYFXFSW-UHFFFAOYSA-N 0.000 description 3
- 102000004190 Enzymes Human genes 0.000 description 3
- 108090000790 Enzymes Proteins 0.000 description 3
- 239000012736 aqueous medium Substances 0.000 description 3
- 230000029087 digestion Effects 0.000 description 3
- 239000000041 non-steroidal anti-inflammatory agent Substances 0.000 description 3
- 229940021182 non-steroidal anti-inflammatory drug Drugs 0.000 description 3
- 239000007787 solid Substances 0.000 description 3
- RQRCJRUUPFZABV-UHFFFAOYSA-N 4-hydroxy-2-methyl-1,2-benzothiazine-3-carboxylic acid Chemical compound C1=CC=C2C(O)=C(C(O)=O)N(C)SC2=C1 RQRCJRUUPFZABV-UHFFFAOYSA-N 0.000 description 2
- GUABFMPMKJGSBQ-UHFFFAOYSA-N 5-methyl-1,3-thiazol-2-amine Chemical compound CC1=CN=C(N)S1 GUABFMPMKJGSBQ-UHFFFAOYSA-N 0.000 description 2
- 102000001708 Protein Isoforms Human genes 0.000 description 2
- 108010029485 Protein Isoforms Proteins 0.000 description 2
- 238000001237 Raman spectrum Methods 0.000 description 2
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 2
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 2
- 230000003247 decreasing effect Effects 0.000 description 2
- 238000004821 distillation Methods 0.000 description 2
- 125000002587 enol group Chemical group 0.000 description 2
- 239000000543 intermediate Substances 0.000 description 2
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 2
- 238000010907 mechanical stirring Methods 0.000 description 2
- 150000007522 mineralic acids Chemical class 0.000 description 2
- 150000007524 organic acids Chemical class 0.000 description 2
- 239000000825 pharmaceutical preparation Substances 0.000 description 2
- 238000000746 purification Methods 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- 229910001220 stainless steel Inorganic materials 0.000 description 2
- 239000010935 stainless steel Substances 0.000 description 2
- SCYULBFZEHDVBN-UHFFFAOYSA-N 1,1-Dichloroethane Chemical compound CC(Cl)Cl SCYULBFZEHDVBN-UHFFFAOYSA-N 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- 206010061218 Inflammation Diseases 0.000 description 1
- 102000004005 Prostaglandin-endoperoxide synthases Human genes 0.000 description 1
- 108090000459 Prostaglandin-endoperoxide synthases Proteins 0.000 description 1
- 230000003110 anti-inflammatory effect Effects 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 239000012043 crude product Substances 0.000 description 1
- 239000003814 drug Substances 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 230000008030 elimination Effects 0.000 description 1
- 238000003379 elimination reaction Methods 0.000 description 1
- 239000000706 filtrate Substances 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 230000002496 gastric effect Effects 0.000 description 1
- 230000009931 harmful effect Effects 0.000 description 1
- 230000002757 inflammatory effect Effects 0.000 description 1
- 230000004054 inflammatory process Effects 0.000 description 1
- 239000003112 inhibitor Substances 0.000 description 1
- 230000005764 inhibitory process Effects 0.000 description 1
- 238000011835 investigation Methods 0.000 description 1
- 230000003902 lesion Effects 0.000 description 1
- 239000002609 medium Substances 0.000 description 1
- 239000012454 non-polar solvent Substances 0.000 description 1
- 229940127557 pharmaceutical product Drugs 0.000 description 1
- 238000011084 recovery Methods 0.000 description 1
- 238000001953 recrystallisation Methods 0.000 description 1
- 150000003431 steroids Chemical class 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
- C07D417/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
- C07D417/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- 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]
-
- 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
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Public Health (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Pharmacology & Pharmacy (AREA)
- Veterinary Medicine (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Pain & Pain Management (AREA)
- Rheumatology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Preparation Of Compounds By Using Micro-Organisms (AREA)
- Cosmetics (AREA)
Priority Applications (21)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| ES200102743A ES2223209B1 (es) | 2001-12-11 | 2001-12-11 | Nuevas formas cristalinas del meloxicam y procedimientos para su preparacion e interconversion. |
| MXPA04005338A MXPA04005338A (es) | 2001-12-11 | 2002-11-19 | Nuevas formas cristalinas del meloxicam y procedimientos para su preparacion e interconversion. |
| JP2003558007A JP2005516030A (ja) | 2001-12-11 | 2002-11-19 | 新規な結晶性の形態のメロキシカム並びにそれらの製造及び相互転換方法 |
| AT02785450T ATE318813T1 (de) | 2001-12-11 | 2002-11-19 | Neue kristalline formen von meloxicam, deren herstellung und verfahren zu deren umwandlung ineinander |
| EP02785450A EP1462451B1 (en) | 2001-12-11 | 2002-11-19 | Novel crystalline forms of meloxicam and the preparation and interconversion methods thereof |
| CA002470164A CA2470164A1 (en) | 2001-12-11 | 2002-11-19 | New crystalline forms of meloxicam and processes for their preparation and interconversion. |
| SI200230288T SI1462451T1 (sl) | 2001-12-11 | 2002-11-19 | Nove kristalne oblike meloksikama in priprava in medsebojno zamenljivi postopki pri le-teh |
| ES02785450T ES2259725T3 (es) | 2001-12-11 | 2002-11-19 | Nuevas formas cristalinas del meloxicam y procedimientos para su preparacion e interconversion. |
| DK02785450T DK1462451T3 (da) | 2001-12-11 | 2002-11-19 | Nye krystallinske former af meloxicam og fremgangsmåder til fremstilling og omdannelse heraf |
| DE60209537T DE60209537T2 (de) | 2001-12-11 | 2002-11-19 | Neue kristalline formen von meloxicam, deren herstellung und verfahren zu deren umwandlung ineinander |
| KR1020047008796A KR100919927B1 (ko) | 2001-12-11 | 2002-11-19 | 멜록시캄의 신규한 결정형 그리고 그들의 제조 및상호전환 방법 |
| HU0402536A HUP0402536A3 (en) | 2001-12-11 | 2002-11-19 | Novel crystalline forms of meloxicam and the preparation and interconversion methods thereof |
| PCT/ES2002/000539 WO2003057692A1 (es) | 2001-12-11 | 2002-11-19 | Nuevas formas cristalinas del meloxicam y procedimientos para su preparacion e interconversion |
| PT02785450T PT1462451E (pt) | 2001-12-11 | 2002-11-19 | Novas formas cristalinas do meloxicam e subsequentes metodos para a sua preparacao e interconversao |
| AU2002350753A AU2002350753B2 (en) | 2001-12-11 | 2002-11-19 | Novel crystalline forms of meloxicam and the preparation and interconversion methods thereof |
| PL02370435A PL370435A1 (en) | 2001-12-11 | 2002-11-19 | Novel crystalline forms of meloxicam and the preparation and interconversion methods thereof |
| NZ533521A NZ533521A (en) | 2001-12-11 | 2002-11-19 | New crystalline forms of meloxicam and processes for their preparation and interconversion |
| US10/314,545 US6692776B2 (en) | 2000-09-06 | 2002-12-09 | Method of repairing or restoring damaged or imperfect hair |
| US10/314,542 US6967248B2 (en) | 2001-12-11 | 2002-12-09 | Crystalline forms of meloxicam and processes for their preparation and interconversion |
| ZA200404475A ZA200404475B (en) | 2001-12-11 | 2004-06-07 | Novel crystalline forms of meloxicam and the preparation and interconversion methods thereof. |
| NO20042936A NO326746B1 (no) | 2001-12-11 | 2004-07-12 | Nye krystallinske former av meloksikam og fremgangsmater for deres fremstilling og interkonversjon |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| ES200102743A ES2223209B1 (es) | 2001-12-11 | 2001-12-11 | Nuevas formas cristalinas del meloxicam y procedimientos para su preparacion e interconversion. |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| ES2223209A1 ES2223209A1 (es) | 2005-02-16 |
| ES2223209B1 true ES2223209B1 (es) | 2005-10-01 |
Family
ID=8499703
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ES200102743A Expired - Fee Related ES2223209B1 (es) | 2000-09-06 | 2001-12-11 | Nuevas formas cristalinas del meloxicam y procedimientos para su preparacion e interconversion. |
| ES02785450T Expired - Lifetime ES2259725T3 (es) | 2001-12-11 | 2002-11-19 | Nuevas formas cristalinas del meloxicam y procedimientos para su preparacion e interconversion. |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ES02785450T Expired - Lifetime ES2259725T3 (es) | 2001-12-11 | 2002-11-19 | Nuevas formas cristalinas del meloxicam y procedimientos para su preparacion e interconversion. |
Country Status (18)
| Country | Link |
|---|---|
| US (1) | US6967248B2 (enExample) |
| EP (1) | EP1462451B1 (enExample) |
| JP (1) | JP2005516030A (enExample) |
| KR (1) | KR100919927B1 (enExample) |
| AT (1) | ATE318813T1 (enExample) |
| AU (1) | AU2002350753B2 (enExample) |
| CA (1) | CA2470164A1 (enExample) |
| DE (1) | DE60209537T2 (enExample) |
| DK (1) | DK1462451T3 (enExample) |
| ES (2) | ES2223209B1 (enExample) |
| HU (1) | HUP0402536A3 (enExample) |
| MX (1) | MXPA04005338A (enExample) |
| NO (1) | NO326746B1 (enExample) |
| NZ (1) | NZ533521A (enExample) |
| PL (1) | PL370435A1 (enExample) |
| PT (1) | PT1462451E (enExample) |
| WO (1) | WO2003057692A1 (enExample) |
| ZA (1) | ZA200404475B (enExample) |
Families Citing this family (21)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US20020035107A1 (en) * | 2000-06-20 | 2002-03-21 | Stefan Henke | Highly concentrated stable meloxicam solutions |
| DE10161077A1 (de) | 2001-12-12 | 2003-06-18 | Boehringer Ingelheim Vetmed | Hochkonzentrierte stabile Meloxicamlösungen zur nadellosen Injektion |
| US8992980B2 (en) | 2002-10-25 | 2015-03-31 | Boehringer Ingelheim Vetmedica Gmbh | Water-soluble meloxicam granules |
| EP1568369A1 (en) | 2004-02-23 | 2005-08-31 | Boehringer Ingelheim Vetmedica Gmbh | Use of meloxicam for the treatment of respiratory diseases in pigs |
| DE102004021281A1 (de) * | 2004-04-29 | 2005-11-24 | Boehringer Ingelheim Vetmedica Gmbh | Verwendung von Meloxicam-Formulierungen in der Veterinärmedizin |
| DE102004030409A1 (de) * | 2004-06-23 | 2006-01-26 | Boehringer Ingelheim Vetmedica Gmbh | Neue Verwendung von Meloxicam in der Veterinärmedizin |
| ITMI20041918A1 (it) | 2004-10-11 | 2005-01-11 | A M S A Anonima Materie Sintetiche Affini Spa | Processo di purificazione di meloxicam |
| HU227359B1 (en) * | 2004-12-18 | 2011-04-28 | Egis Gyogyszergyar Nyilvanosan Mikodi Ruszvunytarsasag | Process for producing meloxicam and meloxicam potassium salt of high purity |
| FR2889847B1 (fr) | 2005-08-18 | 2007-10-05 | Sanofi Aventis Sa | Derives de 5-pyridazinyl-1-azabicyclo[3.2.1]octave, leur preparation en therapeutique. |
| BRPI0617208A2 (pt) * | 2005-09-30 | 2011-07-19 | Boehringer Ingelheim Vetmed | preparação farmacêutica contendo meloxicam |
| GB2443891B (en) * | 2006-11-20 | 2009-04-08 | Norbrook Lab Ltd | Process for the purification of meloxicam |
| WO2009094155A1 (en) * | 2008-01-22 | 2009-07-30 | Thar Pharmaceuticals | In vivo studies of crystalline forms of meloxicam |
| DK2488145T3 (da) * | 2009-10-12 | 2024-07-22 | Boehringer Ingelheim Vetmedica Gmbh | Beholdere til sammensætninger omfattende meloxicam |
| CA2791805A1 (en) | 2010-03-03 | 2011-09-09 | Boehringer Ingelheim Vetmedica Gmbh | Use of meloxicam for the long-term treatment of musculoskeletal disorders in cats |
| US9795568B2 (en) | 2010-05-05 | 2017-10-24 | Boehringer Ingelheim Vetmedica Gmbh | Low concentration meloxicam tablets |
| CN103772378B (zh) * | 2014-01-26 | 2016-02-24 | 悦康药业集团有限公司 | 一种美洛昔康化合物及其片剂 |
| CN109983013A (zh) * | 2016-11-18 | 2019-07-05 | 帕西拉制药有限公司 | 美洛昔康锌复合物微粒多囊脂质体制剂及其制备方法 |
| US20210322316A1 (en) * | 2016-11-18 | 2021-10-21 | Pacira Pharmaceuticals, Inc. | Zinc meloxicam complex microparticles and anesthetic formulations and processes for making the same |
| EP3958841A1 (en) | 2019-04-22 | 2022-03-02 | Mylan Specialty L.P. | Meloxicam co-crystal compositions |
| WO2022097024A1 (en) | 2020-11-06 | 2022-05-12 | Mylan Laboratories Ltd | Pharmaceutical composition comprising meloxicam |
| CN116421567B (zh) * | 2023-04-27 | 2025-02-07 | 浙江萃泽医药科技有限公司 | 一种稳定冻干制剂及其制备方法和应用 |
Family Cites Families (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE2756113A1 (de) * | 1977-12-16 | 1979-06-21 | Thomae Gmbh Dr K | Neue 4-hydroxy-2h-1,2-benzothiazin- 3-carboxamid-1,1-dioxide, verfahren zu ihrer herstellung und diese enthaltende arzneimittel |
| US6355666B1 (en) * | 2000-06-23 | 2002-03-12 | Medinox, Inc. | Protected forms of pharmacologically active agents and uses therefor |
-
2001
- 2001-12-11 ES ES200102743A patent/ES2223209B1/es not_active Expired - Fee Related
-
2002
- 2002-11-19 PL PL02370435A patent/PL370435A1/xx not_active Application Discontinuation
- 2002-11-19 KR KR1020047008796A patent/KR100919927B1/ko not_active Expired - Fee Related
- 2002-11-19 AU AU2002350753A patent/AU2002350753B2/en not_active Ceased
- 2002-11-19 HU HU0402536A patent/HUP0402536A3/hu unknown
- 2002-11-19 AT AT02785450T patent/ATE318813T1/de not_active IP Right Cessation
- 2002-11-19 NZ NZ533521A patent/NZ533521A/en not_active IP Right Cessation
- 2002-11-19 JP JP2003558007A patent/JP2005516030A/ja active Pending
- 2002-11-19 ES ES02785450T patent/ES2259725T3/es not_active Expired - Lifetime
- 2002-11-19 MX MXPA04005338A patent/MXPA04005338A/es active IP Right Grant
- 2002-11-19 CA CA002470164A patent/CA2470164A1/en not_active Abandoned
- 2002-11-19 EP EP02785450A patent/EP1462451B1/en not_active Expired - Lifetime
- 2002-11-19 PT PT02785450T patent/PT1462451E/pt unknown
- 2002-11-19 DE DE60209537T patent/DE60209537T2/de not_active Expired - Lifetime
- 2002-11-19 DK DK02785450T patent/DK1462451T3/da active
- 2002-11-19 WO PCT/ES2002/000539 patent/WO2003057692A1/es not_active Ceased
- 2002-12-09 US US10/314,542 patent/US6967248B2/en not_active Expired - Fee Related
-
2004
- 2004-06-07 ZA ZA200404475A patent/ZA200404475B/xx unknown
- 2004-07-12 NO NO20042936A patent/NO326746B1/no not_active IP Right Cessation
Non-Patent Citations (1)
| Title |
|---|
| LUGER, P. y col. Structure and physicochemical properties of meloxicam, a new NSAID. European Journal of Pharmaceutical Sciences. 1996. Vol. 4, Nº 3, páginas 175-187, ISSN 0928-0987. Resumen; página 177, columna izquierda; página 178, tabla 1; página 185, figura 11. * |
Also Published As
| Publication number | Publication date |
|---|---|
| EP1462451A1 (en) | 2004-09-29 |
| ES2223209A1 (es) | 2005-02-16 |
| ES2259725T3 (es) | 2006-10-16 |
| NO326746B1 (no) | 2009-02-09 |
| KR100919927B1 (ko) | 2009-10-07 |
| KR20040082380A (ko) | 2004-09-24 |
| NO20042936L (no) | 2004-09-13 |
| WO2003057692A1 (es) | 2003-07-17 |
| MXPA04005338A (es) | 2005-03-31 |
| DE60209537T2 (de) | 2006-11-16 |
| DK1462451T3 (da) | 2006-06-12 |
| ZA200404475B (en) | 2005-06-07 |
| PL370435A1 (en) | 2005-05-30 |
| PT1462451E (pt) | 2006-07-31 |
| US20030109701A1 (en) | 2003-06-12 |
| CA2470164A1 (en) | 2003-07-17 |
| NZ533521A (en) | 2005-07-29 |
| ATE318813T1 (de) | 2006-03-15 |
| AU2002350753A1 (en) | 2003-07-24 |
| US6967248B2 (en) | 2005-11-22 |
| DE60209537D1 (de) | 2006-04-27 |
| HUP0402536A3 (en) | 2011-03-28 |
| HUP0402536A2 (hu) | 2005-04-28 |
| JP2005516030A (ja) | 2005-06-02 |
| AU2002350753B2 (en) | 2008-05-08 |
| EP1462451B1 (en) | 2006-03-01 |
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