CA2272402A1 - Granules comprising clavulanate and one or more excipients - Google Patents
Granules comprising clavulanate and one or more excipients Download PDFInfo
- Publication number
- CA2272402A1 CA2272402A1 CA002272402A CA2272402A CA2272402A1 CA 2272402 A1 CA2272402 A1 CA 2272402A1 CA 002272402 A CA002272402 A CA 002272402A CA 2272402 A CA2272402 A CA 2272402A CA 2272402 A1 CA2272402 A1 CA 2272402A1
- Authority
- CA
- Canada
- Prior art keywords
- granules
- clavulanate
- anyone
- excipients
- roller compactor
- 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.)
- Abandoned
Links
- 239000008187 granular material Substances 0.000 title claims abstract description 81
- 239000000546 pharmaceutical excipient Substances 0.000 title claims abstract description 30
- HZZVJAQRINQKSD-UHFFFAOYSA-N Clavulanic acid Natural products OC(=O)C1C(=CCO)OC2CC(=O)N21 HZZVJAQRINQKSD-UHFFFAOYSA-N 0.000 title claims abstract description 21
- HZZVJAQRINQKSD-PBFISZAISA-N clavulanic acid Chemical compound OC(=O)[C@H]1C(=C/CO)/O[C@@H]2CC(=O)N21 HZZVJAQRINQKSD-PBFISZAISA-N 0.000 title claims abstract description 21
- 229940090805 clavulanate Drugs 0.000 title claims abstract description 19
- 238000000034 method Methods 0.000 claims abstract description 26
- 238000007873 sieving Methods 0.000 claims abstract description 19
- 239000008194 pharmaceutical composition Substances 0.000 claims abstract description 4
- ABVRVIZBZKUTMK-JSYANWSFSA-M potassium clavulanate Chemical group [K+].[O-]C(=O)[C@H]1C(=C/CO)/O[C@@H]2CC(=O)N21 ABVRVIZBZKUTMK-JSYANWSFSA-M 0.000 claims description 30
- LSQZJLSUYDQPKJ-NJBDSQKTSA-N amoxicillin Chemical compound C1([C@@H](N)C(=O)N[C@H]2[C@H]3SC([C@@H](N3C2=O)C(O)=O)(C)C)=CC=C(O)C=C1 LSQZJLSUYDQPKJ-NJBDSQKTSA-N 0.000 claims description 22
- 239000003826 tablet Substances 0.000 claims description 20
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 17
- 239000000203 mixture Substances 0.000 claims description 15
- 229960004920 amoxicillin trihydrate Drugs 0.000 claims description 12
- 238000002360 preparation method Methods 0.000 claims description 12
- 229960003022 amoxicillin Drugs 0.000 claims description 10
- LSQZJLSUYDQPKJ-UHFFFAOYSA-N p-Hydroxyampicillin Natural products O=C1N2C(C(O)=O)C(C)(C)SC2C1NC(=O)C(N)C1=CC=C(O)C=C1 LSQZJLSUYDQPKJ-UHFFFAOYSA-N 0.000 claims description 10
- 239000002245 particle Substances 0.000 claims description 10
- 239000010419 fine particle Substances 0.000 claims description 9
- 239000000843 powder Substances 0.000 claims description 9
- 229920000168 Microcrystalline cellulose Polymers 0.000 claims description 7
- 239000011230 binding agent Substances 0.000 claims description 7
- 235000019813 microcrystalline cellulose Nutrition 0.000 claims description 7
- 239000008108 microcrystalline cellulose Substances 0.000 claims description 7
- 229940016286 microcrystalline cellulose Drugs 0.000 claims description 7
- 239000002775 capsule Substances 0.000 claims description 5
- 239000001913 cellulose Substances 0.000 claims description 4
- 235000010980 cellulose Nutrition 0.000 claims description 4
- 229920002678 cellulose Polymers 0.000 claims description 4
- 238000003801 milling Methods 0.000 claims description 4
- 239000002904 solvent Substances 0.000 claims description 4
- 230000035699 permeability Effects 0.000 claims description 3
- 239000006188 syrup Substances 0.000 claims description 3
- 235000020357 syrup Nutrition 0.000 claims description 3
- 239000006186 oral dosage form Substances 0.000 claims description 2
- 230000003134 recirculating effect Effects 0.000 claims 1
- 239000000463 material Substances 0.000 description 10
- 230000000694 effects Effects 0.000 description 8
- HQKMJHAJHXVSDF-UHFFFAOYSA-L magnesium stearate Chemical compound [Mg+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O HQKMJHAJHXVSDF-UHFFFAOYSA-L 0.000 description 8
- 239000011362 coarse particle Substances 0.000 description 7
- 238000005469 granulation Methods 0.000 description 7
- 230000003179 granulation Effects 0.000 description 7
- 238000000354 decomposition reaction Methods 0.000 description 6
- 238000005550 wet granulation Methods 0.000 description 6
- 238000007908 dry granulation Methods 0.000 description 5
- 238000009491 slugging Methods 0.000 description 5
- 238000004090 dissolution Methods 0.000 description 4
- 235000019359 magnesium stearate Nutrition 0.000 description 4
- 238000005056 compaction Methods 0.000 description 3
- 239000013078 crystal Substances 0.000 description 3
- 229940079593 drug Drugs 0.000 description 3
- 239000003814 drug Substances 0.000 description 3
- 239000007903 gelatin capsule Substances 0.000 description 3
- 238000001802 infusion Methods 0.000 description 3
- 238000002156 mixing Methods 0.000 description 3
- 239000003960 organic solvent Substances 0.000 description 3
- 238000009490 roller compaction Methods 0.000 description 3
- 241000237858 Gastropoda Species 0.000 description 2
- TWRXJAOTZQYOKJ-UHFFFAOYSA-L Magnesium chloride Chemical compound [Mg+2].[Cl-].[Cl-] TWRXJAOTZQYOKJ-UHFFFAOYSA-L 0.000 description 2
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 2
- 238000004458 analytical method Methods 0.000 description 2
- 230000003115 biocidal effect Effects 0.000 description 2
- 229960003324 clavulanic acid Drugs 0.000 description 2
- 239000011248 coating agent Substances 0.000 description 2
- 238000000576 coating method Methods 0.000 description 2
- 238000009826 distribution Methods 0.000 description 2
- 239000002552 dosage form Substances 0.000 description 2
- 238000001035 drying Methods 0.000 description 2
- 239000000428 dust Substances 0.000 description 2
- 239000000796 flavoring agent Substances 0.000 description 2
- 235000019634 flavors Nutrition 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 239000011591 potassium Substances 0.000 description 2
- 229910052700 potassium Inorganic materials 0.000 description 2
- 239000000047 product Substances 0.000 description 2
- 150000003839 salts Chemical class 0.000 description 2
- 238000005204 segregation Methods 0.000 description 2
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- 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 description 1
- 239000004480 active ingredient Substances 0.000 description 1
- 239000006067 antibiotic powder Substances 0.000 description 1
- 239000003782 beta lactam antibiotic agent Substances 0.000 description 1
- 239000004067 bulking agent Substances 0.000 description 1
- 239000001110 calcium chloride Substances 0.000 description 1
- 229910001628 calcium chloride Inorganic materials 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 239000007910 chewable tablet Substances 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 239000002178 crystalline material Substances 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 239000002274 desiccant Substances 0.000 description 1
- 239000007884 disintegrant Substances 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 238000011049 filling Methods 0.000 description 1
- 238000005429 filling process Methods 0.000 description 1
- 239000012467 final product Substances 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 230000002209 hydrophobic effect Effects 0.000 description 1
- 239000000314 lubricant Substances 0.000 description 1
- 229910001629 magnesium chloride Inorganic materials 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 239000002491 polymer binding agent Substances 0.000 description 1
- 239000003755 preservative agent Substances 0.000 description 1
- 238000012216 screening Methods 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 239000011780 sodium chloride Substances 0.000 description 1
- FAPWRFPIFSIZLT-UHFFFAOYSA-M sodium chloride Inorganic materials [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 1
- 229940079832 sodium starch glycolate Drugs 0.000 description 1
- 239000008109 sodium starch glycolate Substances 0.000 description 1
- 229920003109 sodium starch glycolate Polymers 0.000 description 1
- 238000001179 sorption measurement Methods 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 235000000346 sugar Nutrition 0.000 description 1
- 150000008163 sugars Chemical class 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 229920001059 synthetic polymer Polymers 0.000 description 1
- 239000007916 tablet composition Substances 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 230000001225 therapeutic effect Effects 0.000 description 1
- 150000004684 trihydrates Chemical class 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
- A61K9/14—Particulate form, e.g. powders, Processes for size reducing of pure drugs or the resulting products, Pure drug nanoparticles
- A61K9/16—Agglomerates; Granulates; Microbeadlets ; Microspheres; Pellets; Solid products obtained by spray drying, spray freeze drying, spray congealing,(multiple) emulsion solvent evaporation or extraction
- A61K9/1605—Excipients; Inactive ingredients
- A61K9/1629—Organic macromolecular compounds
- A61K9/1652—Polysaccharides, e.g. alginate, cellulose derivatives; Cyclodextrin
-
- 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
- A61K31/424—Oxazoles condensed with heterocyclic ring systems, e.g. clavulanic acid
-
- 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
- A61K9/14—Particulate form, e.g. powders, Processes for size reducing of pure drugs or the resulting products, Pure drug nanoparticles
- A61K9/16—Agglomerates; Granulates; Microbeadlets ; Microspheres; Pellets; Solid products obtained by spray drying, spray freeze drying, spray congealing,(multiple) emulsion solvent evaporation or extraction
- A61K9/1682—Processes
- A61K9/1694—Processes resulting in granules or microspheres of the matrix type containing more than 5% of excipient
-
- 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
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
Landscapes
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Epidemiology (AREA)
- Communicable Diseases (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Oncology (AREA)
- Medicinal Preparation (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Investigating Or Analysing Biological Materials (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP97203576.0 | 1997-11-17 | ||
| EP97203576 | 1997-11-17 | ||
| PCT/EP1998/007225 WO1999025343A1 (en) | 1997-11-17 | 1998-11-09 | Granules comprising clavulanate and one or more excipients |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CA2272402A1 true CA2272402A1 (en) | 1999-05-27 |
Family
ID=8228930
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA002272402A Abandoned CA2272402A1 (en) | 1997-11-17 | 1998-11-09 | Granules comprising clavulanate and one or more excipients |
Country Status (13)
| Country | Link |
|---|---|
| EP (1) | EP0973520A1 (ar) |
| JP (1) | JP2001516365A (ar) |
| CN (1) | CN1242705A (ar) |
| AU (1) | AU1337999A (ar) |
| BR (1) | BR9806280A (ar) |
| CA (1) | CA2272402A1 (ar) |
| CO (1) | CO4980893A1 (ar) |
| JO (1) | JO2082B1 (ar) |
| NO (1) | NO993467L (ar) |
| PL (1) | PL334517A1 (ar) |
| TR (1) | TR199901584T1 (ar) |
| WO (1) | WO1999025343A1 (ar) |
| ZA (1) | ZA9810499B (ar) |
Families Citing this family (23)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6294199B1 (en) | 1999-04-13 | 2001-09-25 | Beecham Pharmaceuticals (Pte) Limited | Method of treating a bacterial infection comprising administering amoxycillin |
| US6878386B1 (en) | 1999-04-13 | 2005-04-12 | Beecham Pharmaceuticals (Pte) Limited | Method of treating a bacterial infection comprising amoxycillin and potassium clavulanate |
| US7250176B1 (en) | 1999-04-13 | 2007-07-31 | Beecham Pharmaceuticals (Pte) Limited | Method of treating a bacterial infection |
| US6756057B2 (en) | 2000-10-12 | 2004-06-29 | Beecham Pharmaceuticals (Pte) Limited | Amoxicillin and potassium clavulanate dosage form |
| EP1330236A2 (en) | 2000-10-12 | 2003-07-30 | Beecham Pharmaceuticals (Pte) Limited | Formulation containing amoxicillin |
| GB0031267D0 (en) * | 2000-12-21 | 2001-01-31 | Smithkline Beecham Plc | Novel compositions |
| AT412344B (de) * | 2001-04-12 | 2005-01-25 | Sandoz Ag | Hydrophobisierte teilchen von k-clavulanat |
| AT413983B (de) * | 2001-04-12 | 2006-08-15 | Sandoz Ag | K-clavulanat in der form eines granulates |
| AU2004234176B2 (en) * | 2003-05-02 | 2010-05-13 | Globopharm Pharmazeutische Produktions- Und Handelsgesellschaft M.B.H. | Solid pharmaceutical preparation containing levothyroxine and/or liothyronine salts |
| US8293272B2 (en) * | 2003-05-02 | 2012-10-23 | Globopharm Pharmazeutische Produktions-Und Handelsgesellschaft M.B.H. | Solid pharmaceutical preparation containing levothyroxine and/or liothyronine salts |
| FI20080352A0 (fi) * | 2008-05-09 | 2008-05-09 | Atacama Labs Oy | Prosessi korkean lääkepitoisuuden tabletin valmistamiseksi |
| US8951562B2 (en) | 2006-11-10 | 2015-02-10 | Atacama Labs Oy | Method and apparatus or dry granulation |
| FI20080351A0 (fi) * | 2008-05-09 | 2008-05-09 | Atacama Labs Oy | Prosessi matalan lääkepitoisuuden tabletin valmistamiseksi |
| FI20080346A0 (fi) * | 2008-05-09 | 2008-05-09 | Atacama Labs Oy | Prosessi lisäaineita sisältävän tabletin valmistamiseksi |
| FI20080353A0 (fi) * | 2008-05-09 | 2008-05-09 | Atacama Labs Oy | Prosessi erittäin korkean lääkepitoisuuden tabletin valmistamiseksi |
| FI20070521A7 (fi) | 2006-11-10 | 2008-05-11 | Atacama Labs Oy | Rakeita, tabletteja ja rakeistusmenetelmä |
| FI20080355A0 (fi) * | 2008-05-09 | 2008-05-09 | Atacama Labs Oy | Prosessi metforminia käsittävien tablettien valmistamiseksi |
| CA2723409C (en) | 2008-05-09 | 2016-11-08 | Atacama Labs Oy | Method and apparatus for dry granulation |
| CN104582692A (zh) * | 2012-08-28 | 2015-04-29 | 中化帝斯曼制药有限公司荷兰公司 | 包含抗生素和β-内酰胺酶抑制剂的组合物,其中抗生素和β-内酰胺酶抑制剂中的至少一种是迷你片剂的形式 |
| JP2014062064A (ja) * | 2012-09-21 | 2014-04-10 | Ohara Yakuhin Kogyo Kk | バルサルタン含有錠剤の製造方法 |
| JP6141472B2 (ja) * | 2016-03-02 | 2017-06-07 | 大原薬品工業株式会社 | バルサルタン含有錠剤の製造方法 |
| KR20250026366A (ko) * | 2017-07-05 | 2025-02-25 | 노파르티스 아게 | 신규한 약학적 조성물 |
| CN110051637A (zh) * | 2019-05-21 | 2019-07-26 | 葵花药业集团北京药物研究院有限公司 | 阿莫西林克拉维酸钾制剂及其制备方法 |
Family Cites Families (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE2251250C3 (de) * | 1972-10-19 | 1981-06-25 | Hoechst Ag, 6230 Frankfurt | Verfahren zur Herstellung hochdosierter Antibiotica-Tabletten |
| NZ187013A (en) * | 1977-04-27 | 1985-04-30 | Beecham Group Ltd | 9-amino-9-deoxy-clavulanic acid derivatives and pharmaceutical compositions |
| NZ189022A (en) * | 1977-12-08 | 1981-11-19 | Beecham Group Ltd | Pharmaceutically acceptable particles of clavulanates dispersed in a polymeric binder |
| DE3887179T2 (de) * | 1987-03-02 | 1994-06-16 | Brocades Pharma Bv | Pharmazeutische Zusammensetzung, pharmazeutisches Granulat und Verfahren zu ihrer Herstellung. |
| IL109770A0 (en) * | 1993-05-29 | 1994-11-28 | Smithkline Beecham Corp | Thermal infusion process for preparing controlled release solid dosage forms of medicaments for oral administration and controlled release solid dosage forms of medicaments prepared thereby |
-
1998
- 1998-11-09 TR TR1999/01584T patent/TR199901584T1/xx unknown
- 1998-11-09 AU AU13379/99A patent/AU1337999A/en not_active Abandoned
- 1998-11-09 PL PL98334517A patent/PL334517A1/xx unknown
- 1998-11-09 CN CN98801549A patent/CN1242705A/zh active Pending
- 1998-11-09 CA CA002272402A patent/CA2272402A1/en not_active Abandoned
- 1998-11-09 WO PCT/EP1998/007225 patent/WO1999025343A1/en not_active Ceased
- 1998-11-09 EP EP98956907A patent/EP0973520A1/en not_active Withdrawn
- 1998-11-09 JP JP52751299A patent/JP2001516365A/ja active Pending
- 1998-11-09 BR BR9806280-8A patent/BR9806280A/pt not_active Application Discontinuation
- 1998-11-17 JO JO19982082A patent/JO2082B1/ar active
- 1998-11-17 ZA ZA9810499A patent/ZA9810499B/xx unknown
- 1998-11-17 CO CO98067517A patent/CO4980893A1/es unknown
-
1999
- 1999-07-14 NO NO993467A patent/NO993467L/no not_active Application Discontinuation
Also Published As
| Publication number | Publication date |
|---|---|
| AU1337999A (en) | 1999-06-07 |
| ZA9810499B (en) | 1999-05-24 |
| TR199901584T1 (xx) | 2000-01-21 |
| CO4980893A1 (es) | 2000-11-27 |
| PL334517A1 (en) | 2000-02-28 |
| WO1999025343A1 (en) | 1999-05-27 |
| JP2001516365A (ja) | 2001-09-25 |
| JO2082B1 (ar) | 2000-05-21 |
| EP0973520A1 (en) | 2000-01-26 |
| NO993467D0 (no) | 1999-07-14 |
| BR9806280A (pt) | 2000-02-15 |
| CN1242705A (zh) | 2000-01-26 |
| NO993467L (no) | 1999-07-14 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| CA2272402A1 (en) | Granules comprising clavulanate and one or more excipients | |
| WO1999011261A1 (en) | Granules free of excipients | |
| AU2002237462B2 (en) | Oral pharmaceutical composition of cefpodoxime proxetil | |
| US8632819B2 (en) | Microcrystalline cellulose and calcium carbonate compositions useful as recompactible pharmaceutical excipients | |
| US20110135927A1 (en) | Excipient for compressed tablets comprising novel spherical mannitol | |
| US20040197402A1 (en) | Oxcarbazepine dosage forms | |
| WO2008104996A2 (en) | Water dispersible pharmaceutical formulation and process for preparing the same | |
| AU2002237462A1 (en) | Oral pharmaceutical composition of cefpodoxime proxetil | |
| EP1682096A1 (en) | Process for preparing clopidogrel compositions | |
| DE60306120T2 (de) | Pharmazeutische formulierung, die n-((1-n-butyl-4-piperidinyl)menthyl)-3,4-dihydro-2h-(1,3)oxazino(3,2-a)indol-10-carboxamid oder ein entsprechendes salz hiervon enthält, sowie deren herstellungsprozess, welcher trockengranulierung beinhaltet | |
| MXPA01009808A (es) | Aglomerados por cristalizacion. | |
| HUP0304078A2 (hu) | Tömörítési eljárás nátrium-fenitoin gyógyszerkészítmény előállítására | |
| WO1997033571A1 (fr) | Preparation d'ecadotril a microdispersion et liberation rapides | |
| US8062664B2 (en) | Process for preparing formulations of lipid-regulating drugs | |
| JP4336380B1 (ja) | 水懸濁性を向上させた細粒剤 | |
| JP2000516601A (ja) | 水溶性化合物及びセルロースを含有する粒状物 | |
| JPH10502937A (ja) | フシジン酸錠剤の製法 | |
| MXPA99006619A (en) | Granules comprising clavulanate and one or more excipients | |
| JP2004517111A (ja) | シタロプラムを含有する薬学的調合物 | |
| CA2888856A1 (en) | Dispersible tablet | |
| HK1023949A (en) | Granules comprising clavulanate and one or more excipients | |
| JPH05221853A (ja) | 崩壊性良好な生薬類含有造粒物 | |
| WO1999020277A1 (en) | Rapidly soluble drug composition | |
| CZ1398A3 (cs) | Terapeutické efervescentní kompozice, farmaceutické granuláty a prostředky, způsoby jejich přípravy a použití | |
| CN112190580A (zh) | 用于制备依折麦布片的方法及依折麦布片 |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| FZDE | Discontinued | ||
| FZDE | Discontinued |
Effective date: 20021112 |