FI115443B - Förfarande för framställning av orala sammansättningar av ett antimykotikum - Google Patents

Förfarande för framställning av orala sammansättningar av ett antimykotikum Download PDF

Info

Publication number
FI115443B
FI115443B FI961436A FI961436A FI115443B FI 115443 B FI115443 B FI 115443B FI 961436 A FI961436 A FI 961436A FI 961436 A FI961436 A FI 961436A FI 115443 B FI115443 B FI 115443B
Authority
FI
Finland
Prior art keywords
composition
cyclodextrin
process according
itraconazole
propylene glycol
Prior art date
Application number
FI961436A
Other languages
English (en)
Finnish (fi)
Other versions
FI961436A (sv
FI961436A0 (sv
Inventor
Marc Karel Jozef Francois
Willy Maria Albert Carlo Dries
Original Assignee
Janssen Pharmaceutica Nv
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Janssen Pharmaceutica Nv filed Critical Janssen Pharmaceutica Nv
Publication of FI961436A publication Critical patent/FI961436A/sv
Publication of FI961436A0 publication Critical patent/FI961436A0/sv
Application granted granted Critical
Publication of FI115443B publication Critical patent/FI115443B/sv

Links

Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K9/00Medicinal preparations characterised by special physical form
    • A61K9/0087Galenical forms not covered by A61K9/02 - A61K9/7023
    • A61K9/0095Drinks; Beverages; Syrups; Compositions for reconstitution thereof, e.g. powders or tablets to be dispersed in a glass of water; Veterinary drenches
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/495Heterocyclic 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
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K47/00Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
    • A61K47/30Macromolecular organic or inorganic compounds, e.g. inorganic polyphosphates
    • A61K47/36Polysaccharides; Derivatives thereof, e.g. gums, starch, alginate, dextrin, hyaluronic acid, chitosan, inulin, agar or pectin
    • A61K47/40Cyclodextrins; Derivatives thereof
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K47/00Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
    • A61K47/50Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates
    • A61K47/69Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the conjugate being characterised by physical or galenical forms, e.g. emulsion, particle, inclusion complex, stent or kit
    • A61K47/6949Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the conjugate being characterised by physical or galenical forms, e.g. emulsion, particle, inclusion complex, stent or kit inclusion complexes, e.g. clathrates, cavitates or fullerenes
    • A61K47/6951Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the conjugate being characterised by physical or galenical forms, e.g. emulsion, particle, inclusion complex, stent or kit inclusion complexes, e.g. clathrates, cavitates or fullerenes using cyclodextrin
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • A61P31/04Antibacterial agents
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • A61P31/10Antimycotics
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B82NANOTECHNOLOGY
    • B82YSPECIFIC USES OR APPLICATIONS OF NANOSTRUCTURES; MEASUREMENT OR ANALYSIS OF NANOSTRUCTURES; MANUFACTURE OR TREATMENT OF NANOSTRUCTURES
    • B82Y5/00Nanobiotechnology or nanomedicine, e.g. protein engineering or drug delivery

Landscapes

  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Medicinal Chemistry (AREA)
  • General Health & Medical Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Epidemiology (AREA)
  • Engineering & Computer Science (AREA)
  • Nanotechnology (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • General Engineering & Computer Science (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Molecular Biology (AREA)
  • Medical Informatics (AREA)
  • Biotechnology (AREA)
  • Biophysics (AREA)
  • Inorganic Chemistry (AREA)
  • Communicable Diseases (AREA)
  • Oncology (AREA)
  • Crystallography & Structural Chemistry (AREA)
  • General Chemical & Material Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Organic Chemistry (AREA)
  • Medicinal Preparation (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
  • Agricultural Chemicals And Associated Chemicals (AREA)

Claims (7)

1. Förfarande för framställning av en oralt admi-nistrerbar, terapeutiskt användbar, vattenhaltig komposi-5 tion, vilken komposition innehäller: (a) itrakonazol eller saperkonazol, (b) en tillräcklig mängd cyklodextrin eller ett derivat därav för att fungera som lösningsmedel för itrakonazol eller saperkonazol, 10 (c) ett surt vattenmedium som flytande bulkbärare, (d) alkoholmedlösningsmedel som har valts frän gruppen etanol, propylenglykol och glycerol, (e) tillräckliga mängder av ett eller flera farma-ceutiskt godtagbara intensivsötningsmedel och ett eller 15 flera bulksötningsmedel, (f) en tillräcklig mängd av ett eller flera farma-ceutiskt godtagbara aromämnen för att maskera den vatten-haltiga lösningens smak, kännetecknat av att det omfattar steg, i 20 vilka: (i) ett aktivt ämne upplöses i alkoholmedlösnings-: medlet och en syra, *; (ii) cyklodextrin upplöses i vatten och i denna j. lösning tillsättes den i punkt (i) framställda lösningen 25 under samtidig omröring tili en homogen blandning, ♦ · (iii) sötningsmedlet (-medlen) och aromämnet !!! (-ämnena) tillsättes.
' 2. Förfarande enligt patentkrav 1, känneteck nat av att man framställer en komposition, i vilken cyk- • « · : 30 lodextrin är hydroxipropyl- β-cyklodextrin, vars MS-värde II» är i omrädet 0,35 - 3 och som innehäller under 5 % icke- : substituerat β-cyklodextrin. t » · t···,
3. Förfarande enligt patentkrav 1, känneteck- » · nat av att man framställer en komposition, i vilken al-; i 35 koholmedlösningsmedlet är propylenglykol. 115443
4. Förfarande enligt patentkrav 1, känneteck-n a t av att man framställer en komposition, vars pH-värde är 2,0 ± 0,1.
5. Förfarande enligt patentkrav 1, känneteck-5 nat av att intensivsötningsmedlet väljs frän gruppen sackarin, natrium- eller kalciumsackarin och bulksötnings-medlet väljs frän gruppen sorbitol, mannitol, fruktos, sackaros, maltos, glukos, karamell eller honung.
6. Förfarande enligt patentkrav 1, känneteck-10 nat av att man framställer en komposition som omfattar som vikt- eller volymprocent beräknat pä kompositionens totalvolym (a) 4 vikt/volym-% itrakonazol, (b) 60 vikt/volym-% hydroxipropyl-p-cyklodextrin, 15 (c) 10 volym/volym-% propylenglykol, (d) syra och bas för regiering av komposit ionens pH-värde tili intervallet 2,0 ± 0,1, (e) 0,08 vikt/volym-% natriumsackarin, (f) upp till 1 vikt/volym-% av ett eller flera 20 aromämnen och (g) vatten.
>* 7. Förfarande enligt patentkrav 1, känneteck- .* n a t av att man framställer en komposition som omfattar g’ som vikt- eller volymprocent beräknat pä kompositionens 25 totalvolym ; (a) 1 vikt/volym-% itrakonazol eller saperkonazol, (b) 40 vikt/volym-% hydroxipropyl^-cyklodextrin, (c) 10 volym/volym-% propylenglykol, : ,·, (d) syra och bas för regiering av kompositionens / 30 pH-värde tili intervallet 2,0 ± 0,1, » I (e) 0,06 vikt/volym-% natriumsackarin, » · i (f) 19 volym/volym-% av icke-kristalliserande lös- : : ning av sorbitol (70 %), 115443 (g) upp till 1 vikt/volym-% av ett eller flera aromämnen, (h) 0,02 vikt/volym-% karamellsötningsmedel och (i) vatten. » · t 1 t t 1 • · ♦ » · • · I ( I > * « t »
FI961436A 1993-09-30 1996-03-29 Förfarande för framställning av orala sammansättningar av ett antimykotikum FI115443B (sv)

Applications Claiming Priority (4)

Application Number Priority Date Filing Date Title
US12950493A 1993-09-30 1993-09-30
US12950493 1993-09-30
EP9403169 1994-09-22
PCT/EP1994/003169 WO1995008993A1 (en) 1993-09-30 1994-09-22 Oral formulations of an antifungal

Publications (3)

Publication Number Publication Date
FI961436A FI961436A (sv) 1996-03-29
FI961436A0 FI961436A0 (sv) 1996-03-29
FI115443B true FI115443B (sv) 2005-05-13

Family

ID=22440301

Family Applications (1)

Application Number Title Priority Date Filing Date
FI961436A FI115443B (sv) 1993-09-30 1996-03-29 Förfarande för framställning av orala sammansättningar av ett antimykotikum

Country Status (31)

Country Link
US (1) US5707975A (sv)
EP (1) EP0721337B1 (sv)
JP (1) JP3034048B2 (sv)
CN (1) CN1086579C (sv)
AP (1) AP630A (sv)
AT (1) ATE209916T1 (sv)
AU (1) AU692180B2 (sv)
CA (1) CA2170622C (sv)
CY (1) CY2272B1 (sv)
CZ (1) CZ288026B6 (sv)
DE (1) DE69429359T2 (sv)
DK (1) DK0721337T3 (sv)
ES (1) ES2169087T3 (sv)
FI (1) FI115443B (sv)
HK (1) HK1010689A1 (sv)
HU (1) HU221632B1 (sv)
IL (1) IL111093A (sv)
MY (1) MY111136A (sv)
NO (1) NO308985B1 (sv)
NZ (1) NZ273619A (sv)
OA (1) OA10276A (sv)
PH (1) PH31594A (sv)
PL (1) PL313731A1 (sv)
PT (1) PT721337E (sv)
RO (1) RO115114B1 (sv)
RU (1) RU2118899C1 (sv)
SG (1) SG48826A1 (sv)
SK (1) SK282627B6 (sv)
TW (1) TW349870B (sv)
WO (1) WO1995008993A1 (sv)
ZA (1) ZA947619B (sv)

Families Citing this family (41)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
ES2243994T5 (es) 1996-04-19 2009-10-29 Grifols Inc. Procedimiento para la inactivacion virica de proteinas de la sangre liofilizadas.
KR20060066753A (ko) * 1997-10-22 2006-06-16 젠스 포니카우 진균류에 의한 점막염을 국소 치료하기 위한 항진균제의용도
US6683100B2 (en) 1999-01-19 2004-01-27 Novartis Ag Organic compounds
US6194181B1 (en) 1998-02-19 2001-02-27 Novartis Ag Fermentative preparation process for and crystal forms of cytostatics
CA2362728C (en) 1999-03-24 2009-06-23 Fmc Corporation Improved aqueous solubility pharmaceutical formulations
ATE313319T1 (de) 1999-03-31 2006-01-15 Janssen Pharmaceutica Nv Vorgelatinierte stärke in einer formulierung mit gesteuerter freigabe
AU5975700A (en) * 1999-07-02 2001-01-22 Janssen Pharmaceutica N.V. Nasal formulation of an antifungal
CA2291346A1 (en) 1999-11-26 2001-05-26 Bernard Charles Sherman Antifungal solutions
US6673373B2 (en) 2001-02-01 2004-01-06 Carlsbad Technology Inc. Antifungal formulation and the methods for manufacturing and using the same
EP1372662A1 (en) * 2001-03-05 2004-01-02 Ortho-Mcneil Pharmaceutical, Inc. Taste masked liquid pharmaceutical compositions
CA2363376A1 (en) * 2001-11-16 2003-05-16 Bernard Charles Sherman Solid pharmaceutical compositions for oral administration comprising itraconazole
US7446107B2 (en) * 2002-02-15 2008-11-04 Transform Pharmaceuticals, Inc. Crystalline forms of conazoles and methods of making and using the same
US7790905B2 (en) * 2002-02-15 2010-09-07 Mcneil-Ppc, Inc. Pharmaceutical propylene glycol solvate compositions
WO2003074474A2 (en) * 2002-03-01 2003-09-12 University Of South Florida Multiple-component solid phases containing at least one active pharmaceutical ingredient
US7927613B2 (en) 2002-02-15 2011-04-19 University Of South Florida Pharmaceutical co-crystal compositions
US20100311701A1 (en) * 2002-02-15 2010-12-09 Transform Pharmaceuticals, Inc Pharmaceutical Co-Crystal Compositions
EP1511490A4 (en) * 2002-05-31 2009-03-11 Transform Pharmaceuticals Inc NOVEL CONAZOLE CRYSTALLINE FORMS AND RELATED METHODS, PHARMACEUTICAL COMPOSITIONS AND METHODS
US20070059356A1 (en) * 2002-05-31 2007-03-15 Almarsson Oern Pharmaceutical co-crystal compositions of drugs such as carbamazepine, celecoxib, olanzapine, itraconazole, topiramate, modafinil, 5-fluorouracil, hydrochlorothiazide, acetaminophen, aspirin, flurbiprofen, phenytoin and ibuprofen
CA2489984A1 (en) * 2002-06-21 2003-12-31 Transform Pharmaceuticals, Inc. Pharmaceutical compositions with improved dissolution
WO2007014130A2 (en) * 2005-07-21 2007-02-01 Nomir Medical Technologies, Inc. Near infrared microbial elimination laser system (nimels)
CN1255105C (zh) * 2002-12-17 2006-05-10 上海医药工业研究院 齐拉西酮及其盐的水溶性包合物及其制备方法
US8183290B2 (en) 2002-12-30 2012-05-22 Mcneil-Ppc, Inc. Pharmaceutically acceptable propylene glycol solvate of naproxen
CA2440172C (en) * 2003-09-05 2011-01-11 Bernard Charles Sherman Itraconazole solution
US20050074494A1 (en) * 2003-10-06 2005-04-07 Xiu-Xiu Cheng Itraconazole immediate release formulation
US20050118265A1 (en) * 2003-11-28 2005-06-02 Anandi Krishnan Antifungal oral dosage forms and the methods for preparation
EP1691801A4 (en) * 2003-12-08 2009-12-09 Univ Arizona State SYNERGISTIC ANTICANCER COMPOSITIONS
GR1005154B (el) 2005-02-09 2006-03-13 Verisfield (Uk) Ltd. Σταθερες φαρμακευτικες συνθεσεις ιτρακοναζολης σευδατικο περιβαλλον
WO2007047253A2 (en) * 2005-10-11 2007-04-26 Eastman Chemical Company Pharmaceutical formulations of cyclodextrins and antifungal azole compounds
CL2007002026A1 (es) * 2006-07-13 2008-06-06 Los Angeles Biomed Res Inst Composicion que comprende al menos un compuesto quelante de hierro y al menos un agente antifungico; y metodo para el tratamiento o prevencion de una condicion fungica.
CA2658521C (en) 2006-12-04 2015-06-09 Supernus Pharmaceuticals, Inc. Enhanced immediate release formulations of topiramate
EP2257160B1 (en) 2008-02-21 2017-07-05 Sequoia Pharmaceuticals, Inc. Diamide inhibitors of cytochrome p450
US20100009009A1 (en) 2008-07-10 2010-01-14 Micropure, Inc. Method and composition for prevention and treatment of oral fungal infections
US20100233101A1 (en) 2009-02-13 2010-09-16 Micropure, Inc. Composition and method for the oxidative consumption of salivary biomolecules
US20120093828A1 (en) 2009-03-19 2012-04-19 Ibrahim Ashraf S Vaccine compositions and methods for treatment of mucormycosis and other fungal diseases
CA2821823C (en) * 2010-12-16 2019-05-07 Board Of Regents, The University Of Texas System Azole pharmaceutical formulations for parenteral administration and methods for preparing and using the same as treatment of diseases sensitive to azole compounds
CN102670490A (zh) * 2012-05-10 2012-09-19 南京特丰药业股份有限公司 一种伊曲康唑口服溶液及其制备方法
CN103230363A (zh) * 2013-03-29 2013-08-07 湖北凤凰白云山药业有限公司 一种抗真菌的口服溶液
CA3020197A1 (en) 2017-09-01 2019-03-01 Micropure, Inc. Aliphatic anionic compounds and oxidative compounds with improved stability and efficacy for use in pharmaceutical compositions
RU2707286C1 (ru) * 2019-07-02 2019-11-26 Федеральное государственное бюджетное образовательное учреждение высшего образования "Пермский государственный национальный исследовательский университет" Фармацевтическая противогрибковая композиция на основе производного хлорфенилбутандиона и способ её получения
CN114191386B (zh) * 2021-12-26 2024-03-12 苏州海景医药科技有限公司 一种波生坦口服溶液的制备方法
CN114191387A (zh) * 2021-12-26 2022-03-18 苏州海景医药科技有限公司 一种伏立康唑口服液的制备方法

Family Cites Families (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3459731A (en) * 1966-12-16 1969-08-05 Corn Products Co Cyclodextrin polyethers and their production
US4267179A (en) * 1978-06-23 1981-05-12 Janssen Pharmaceutica, N.V. Heterocyclic derivatives of (4-phenylpiperazin-1-yl-aryloxymethyl-1,3-dioxolan-2-yl)methyl-1H-imidazoles and 1H-1,2,4-triazoles
US4383992A (en) * 1982-02-08 1983-05-17 Lipari John M Water-soluble steroid compounds
US4659696A (en) * 1982-04-30 1987-04-21 Takeda Chemical Industries, Ltd. Pharmaceutical composition and its nasal or vaginal use
DE3346123A1 (de) * 1983-12-21 1985-06-27 Janssen Pharmaceutica, N.V., Beerse Pharmazeutische praeparate von in wasser schwerloeslichen oder instabilen arzneistoffen und verfahren zu ihrer herstellung
US4863737A (en) * 1985-05-01 1989-09-05 University Of Utah Compositions and methods of manufacture of compressed powder medicaments
US4883785A (en) * 1984-07-27 1989-11-28 Chow Wing Sun Complex of anti-fungal agent and cyclodextrin and method
US4870060A (en) * 1985-03-15 1989-09-26 Janssen Pharmaceutica Derivatives of γ-cylodextrin
GB8506792D0 (en) * 1985-03-15 1985-04-17 Janssen Pharmaceutica Nv Derivatives of y-cyclodextrin
US4916134A (en) * 1987-03-25 1990-04-10 Janssen Pharmacuetica N.V. 4-[4-[4-[4-[[2-(2,4-difluorophenyl)-2-(1H-azolylmethyl)-1,3-dioxolan-4-yl]me]phenyl]-1-piperazinyl]phenyl]triazolones
US5002935A (en) * 1987-12-30 1991-03-26 University Of Florida Improvements in redox systems for brain-targeted drug delivery
AU609242B2 (en) * 1988-01-29 1991-04-26 Novartis Ag Cyclosporin compositions
ES2158859T3 (es) * 1992-03-18 2001-09-16 Janssen Pharmaceutica Nv Estereoisomeros itraconazol y saperconazol.

Also Published As

Publication number Publication date
CY2272B1 (en) 2003-07-04
HUT74378A (en) 1996-12-30
CN1086579C (zh) 2002-06-26
WO1995008993A1 (en) 1995-04-06
RO115114B1 (ro) 1999-11-30
NZ273619A (en) 1997-06-24
CZ82396A3 (en) 1996-06-12
EP0721337A1 (en) 1996-07-17
HK1010689A1 (en) 1999-06-25
CN1136776A (zh) 1996-11-27
JPH09502989A (ja) 1997-03-25
ATE209916T1 (de) 2001-12-15
HU9600804D0 (en) 1996-05-28
AP630A (en) 1998-03-10
MY111136A (en) 1999-08-30
ES2169087T3 (es) 2002-07-01
IL111093A (en) 2001-01-28
DE69429359T2 (de) 2002-07-25
SK282627B6 (sk) 2002-10-08
OA10276A (en) 1997-10-07
US5707975A (en) 1998-01-13
FI961436A (sv) 1996-03-29
NO961233L (no) 1996-03-27
FI961436A0 (sv) 1996-03-29
AP9600792A0 (en) 1996-04-30
HU221632B1 (hu) 2002-12-28
JP3034048B2 (ja) 2000-04-17
AU7697994A (en) 1995-04-18
CA2170622A1 (en) 1995-04-06
PH31594A (en) 1998-11-03
AU692180B2 (en) 1998-06-04
ZA947619B (en) 1996-03-29
EP0721337B1 (en) 2001-12-05
NO308985B1 (no) 2000-11-27
RU2118899C1 (ru) 1998-09-20
CZ288026B6 (cs) 2001-04-11
TW349870B (en) 1999-01-11
PL313731A1 (en) 1996-07-22
CA2170622C (en) 1999-07-27
SK39996A3 (en) 1996-12-04
NO961233D0 (no) 1996-03-27
SG48826A1 (en) 1998-05-18
PT721337E (pt) 2002-05-31
DK0721337T3 (da) 2002-03-25
DE69429359D1 (de) 2002-01-17
IL111093A0 (en) 1994-11-28

Similar Documents

Publication Publication Date Title
FI115443B (sv) Förfarande för framställning av orala sammansättningar av ett antimykotikum
DK175288B1 (da) Farmaceutiske midler indeholdende lægemidler, der er ustabile eller sparsomt oplöselige i vand, og fremgangsmåder til deres fremstilling
US6407079B1 (en) Pharmaceutical compositions containing drugs which are instable or sparingly soluble in water and methods for their preparation
EP0900088B1 (en) Inclusion complexes of aryl-heterocyclic salts
EP0759741B1 (en) Mucoadhesive emulsions containing cyclodextrin
FI84076B (fi) Nya derivat av -cyklodextrin och deras framstaellning.
US6699849B1 (en) Cyclodextrin complexes of benzodiazepines
US20060193783A1 (en) Low dose corticosteroid composition
US6077871A (en) Droloxifene pharmaceutical compositions
WO2001001955A1 (en) Nasal formulation of an antifungal
US20190183891A1 (en) Voriconazole inclusion complexes
CN114191387A (zh) 一种伏立康唑口服液的制备方法
FI86507C (sv) Förfarande för framställnig av terapeutiska kompositioner innehållande -cyklodextrinderivat

Legal Events

Date Code Title Description
FG Patent granted

Ref document number: 115443

Country of ref document: FI

MA Patent expired