DK200900284A - Krystallinsk base af escitalopram og smeltetabletter indeholdende escitalopram base - Google Patents

Krystallinsk base af escitalopram og smeltetabletter indeholdende escitalopram base Download PDF

Info

Publication number
DK200900284A
DK200900284A DKPA200900284A DKPA200900284A DK200900284A DK 200900284 A DK200900284 A DK 200900284A DK PA200900284 A DKPA200900284 A DK PA200900284A DK PA200900284 A DKPA200900284 A DK PA200900284A DK 200900284 A DK200900284 A DK 200900284A
Authority
DK
Denmark
Prior art keywords
active pharmaceutical
tablet according
melting
water
soluble filler
Prior art date
Application number
DKPA200900284A
Other languages
English (en)
Inventor
Dancer Robert James
Petersen Hans
Nielsen Ole
Rock Michael Harold
Liljegren Ken
Eliassen Helle
Original Assignee
Lundbeck & Co As H
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
Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=37546630&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=DK200900284(A) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Lundbeck & Co As H filed Critical Lundbeck & Co As H
Priority to DKPA200900284A priority Critical patent/DK200900284A/da
Publication of DK200900284A publication Critical patent/DK200900284A/da

Links

Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/21Esters, e.g. nitroglycerine, selenocyanates
    • A61K31/215Esters, e.g. nitroglycerine, selenocyanates of carboxylic acids
    • A61K31/216Esters, e.g. nitroglycerine, selenocyanates of carboxylic acids of acids having aromatic rings, e.g. benactizyne, clofibrate
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D307/00Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom
    • C07D307/77Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom ortho- or peri-condensed with carbocyclic rings or ring systems
    • C07D307/87Benzo [c] furans; Hydrogenated benzo [c] furans
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/335Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin
    • A61K31/34Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin having five-membered rings with one oxygen as the only ring hetero atom, e.g. isosorbide
    • A61K31/343Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin having five-membered rings with one oxygen as the only ring hetero atom, e.g. isosorbide condensed with a carbocyclic ring, e.g. coumaran, bufuralol, befunolol, clobenfurol, amiodarone
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K9/00Medicinal preparations characterised by special physical form
    • A61K9/20Pills, tablets, discs, rods
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/24Antidepressants
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07BGENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
    • C07B63/00Purification; Separation; Stabilisation; Use of additives

Landscapes

  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Organic Chemistry (AREA)
  • General Health & Medical Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • Medicinal Chemistry (AREA)
  • Animal Behavior & Ethology (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Epidemiology (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Engineering & Computer Science (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Emergency Medicine (AREA)
  • Neurology (AREA)
  • Biomedical Technology (AREA)
  • Neurosurgery (AREA)
  • Psychiatry (AREA)
  • Pain & Pain Management (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Medicinal Preparation (AREA)
  • Furan Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)

Abstract

Den foreliggende opfindelse angår en smeltetablet, der har en hårdhed på mindst 22 N og en oral desintegrationstid på mindre end 120 s, og som indeholder en aktiv farmaceutisk bestanddel adsorberet på et vandopløseligt fyldstof, hvor den aktive farmaceutiske bestanddel har et smeltepunkt i området 40-1 00 °C, såvel som en fremgangsmåde til fremstilling af en sådan smeltetablet.

Claims (11)

1. Smeltetablet, der har en hårdhed på mindst 22 N og en oral desintegrationstid på mindre end 120 s, og som omfatter en aktiv farmaceutisk bestanddel adsorberet på et vandopløseligt fyldstof, ét eller flere desintegrationsmidler og eventuelt yderligere vandopløseligt fyldstof, hvor den aktive farmaceutiske bestanddel har et smeltepunkt i området 40-100 °C.
2. Smeltetablet ifølge krav 1, kendetegnet ved, at den aktive farmaceutiske bestanddel har et smeltepunkt i området 40-90 °C.
3. Smeltetablet ifølge krav 1 eller 2, kendetegnet ved, at den aktive farmaceutiske bestanddel er valgt fra gruppen bestående af escitalopram, ethosuximid, trimethadion, chlorambucil, disulfiram, fenofibrat, guaifenesin, lomustin, carisoprodol og perphenazin.
4. Smeltetablet ifølge krav 3, kendetegnet ved, at den aktive farmaceutiske bestanddel er escitalopram.
5. Smeltetablet ifølge et hvilket som helst af kravene 1-4, kendetegnet ved, at det vandopløselige fyldstof er valgt fra gruppen bestående af monosaccharider, disaccharider, sukkeralkoholer og polysaccharider.
6. Smeltetablet ifølge krav 5, kendetegnet ved, at det vandopløselige fyldstof er valgt fra gruppen bestående af mannitol, sorbitol, glucose, mannose og lactose.
7. Smeltetablet ifølge et hvilket som helst af kravene 1-6, kendetegnet ved, at den har en hårdhed på mindst 22 N.
8. Smeltetablet ifølge et hvilket som helst af kravene 1-7, kendetegnet ved, at den har en oral desintegrationstid på mindre end 60 s.
9. Smeltetablet ifølge et hvilket som helst af kravene 1-8, kendetegnet ved, at desintegrationsmidlerne er valgt fra gruppen bestående af mi kro krysta I li nsk cellulose, natriumstivelsesglycolat, croscarmellose-natrium, crospovidon og povidon.
10. Smeltetablet ifølge et hvilket som helst af kravene 1-9, kendetegnet ved, at den har en slidstyrke på ikke mere end 1 %.
11. Fremgangsmåde til fremstilling af en smeltetablet ifølge et hvilket som helst af kravene 1-10, der omfatter: a) blanding af det vandopløselige fyldstof og den aktive farmaceutiske bestanddel ved en temperatur over, omkring eller lidt under den aktive farmaceutiske bestanddels smeltepunkt, hvorved den aktive farmaceutiske bestanddel adsorberes på det vandopløselige fyldstof; b) efterfulgt af afkøling til en temperatur under 40 °C; c) blanding af blandingen af den aktive farmaceutiske bestanddel og det vandopløselige fyldstof med ét eller flere desintegrationsmidler og eventuelt andre hjælpestoffer og d) presning af blandingen til tabletter med en hårdhed på mindst 22 N.
DKPA200900284A 2005-06-22 2009-02-27 Krystallinsk base af escitalopram og smeltetabletter indeholdende escitalopram base DK200900284A (da)

Priority Applications (1)

Application Number Priority Date Filing Date Title
DKPA200900284A DK200900284A (da) 2005-06-22 2009-02-27 Krystallinsk base af escitalopram og smeltetabletter indeholdende escitalopram base

Applications Claiming Priority (6)

Application Number Priority Date Filing Date Title
DKPA200500912 2005-06-22
DK200500912 2005-06-22
DK200800075 2008-01-21
DK200800075A DK200800075A (da) 2005-06-22 2008-01-21 Krystallinsk base af escitalopram og orodispergerbare tabletter indeholdende escitaloprambase
DKPA200900284A DK200900284A (da) 2005-06-22 2009-02-27 Krystallinsk base af escitalopram og smeltetabletter indeholdende escitalopram base
DK200900284 2009-02-27

Publications (1)

Publication Number Publication Date
DK200900284A true DK200900284A (da) 2009-02-27

Family

ID=37546630

Family Applications (3)

Application Number Title Priority Date Filing Date
DK06742481.2T DK1896439T4 (da) 2005-06-22 2006-06-22 Krystallinsk base af escitalopram og orodispergerbare tabletter, der omfatter escitaloprambase
DK200800075A DK200800075A (da) 2005-06-22 2008-01-21 Krystallinsk base af escitalopram og orodispergerbare tabletter indeholdende escitaloprambase
DKPA200900284A DK200900284A (da) 2005-06-22 2009-02-27 Krystallinsk base af escitalopram og smeltetabletter indeholdende escitalopram base

Family Applications Before (2)

Application Number Title Priority Date Filing Date
DK06742481.2T DK1896439T4 (da) 2005-06-22 2006-06-22 Krystallinsk base af escitalopram og orodispergerbare tabletter, der omfatter escitaloprambase
DK200800075A DK200800075A (da) 2005-06-22 2008-01-21 Krystallinsk base af escitalopram og orodispergerbare tabletter indeholdende escitaloprambase

Country Status (39)

Country Link
EP (3) EP1896439B2 (da)
JP (5) JP4906852B2 (da)
KR (5) KR20110084341A (da)
CN (2) CN101189220A (da)
AR (2) AR055062A1 (da)
AT (3) AT10983U1 (da)
AU (2) AU2006261452B2 (da)
BG (1) BG66086B1 (da)
BR (1) BRPI0612295A2 (da)
CA (2) CA2612827C (da)
CY (1) CY1112392T1 (da)
CZ (3) CZ299906B6 (da)
DE (2) DE602006019961D1 (da)
DK (3) DK1896439T4 (da)
EA (2) EA201001108A1 (da)
EE (1) EE00773U1 (da)
ES (2) ES2319073B1 (da)
FI (2) FI20080548A7 (da)
GB (2) GB2442160B (da)
HR (1) HRP20110093T4 (da)
HU (1) HUP0800135A3 (da)
IL (1) IL187454A0 (da)
IS (1) IS8705A (da)
LT (1) LT5550B (da)
LV (1) LV13677B (da)
MX (1) MX2007015328A (da)
MY (2) MY143239A (da)
NO (2) NO20080359L (da)
PL (2) PL1896439T5 (da)
PT (1) PT1896439E (da)
RS (1) RS51575B2 (da)
SG (1) SG169358A1 (da)
SI (1) SI1896439T2 (da)
SK (1) SK500402007A3 (da)
TR (2) TR201000625T1 (da)
TW (2) TWI347942B (da)
UA (1) UA86536C2 (da)
WO (1) WO2006136169A2 (da)
ZA (2) ZA200711066B (da)

Families Citing this family (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB0123400D0 (en) 2001-09-28 2001-11-21 Novartis Ag Organic compounds
WO2008059514A2 (en) * 2006-07-31 2008-05-22 Cadila Healthcare Limited Process for preparing escitalopram
WO2008104880A2 (en) * 2007-03-01 2008-09-04 Aurobindo Pharma Limited Stable solid dosage forms of an antidepressant
EP2595979B1 (en) 2010-07-23 2016-04-06 H. Lundbeck A/S Process for the purification of pharmaceutically acceptable salts of escitalopram
CN103360353A (zh) * 2013-08-07 2013-10-23 中国药科大学 草酸艾司西酞普兰杂质的制备方法
JP2018016569A (ja) * 2016-07-26 2018-02-01 株式会社トクヤマ (1s)−1−[3−(ジメチルアミノ)プロピル]−1−(4−フルオロフェニル)−1,3−ジヒドロイソベンゾフラン−5−カルボニトリル蓚酸塩の製造方法
WO2018190294A1 (ja) * 2017-04-10 2018-10-18 東和薬品株式会社 エスシタロプラム医薬組成物
CN110711198B (zh) * 2018-07-12 2022-03-15 山东大学 D-甘露糖在制备抗抑郁药物中的应用
KR102331187B1 (ko) 2019-04-09 2021-11-26 주식회사 라이트팜텍 에스시탈로프람을 함유하는 안정성이 우수한 경구용 액제 조성물 및 그의 제조방법
US20240100012A1 (en) * 2021-01-18 2024-03-28 Mark Hasleton Pharmaceutical dosage form

Family Cites Families (39)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB1526331A (en) 1976-01-14 1978-09-27 Kefalas As Phthalanes
GB8814057D0 (en) 1988-06-14 1988-07-20 Lundbeck & Co As H New enantiomers & their isolation
JPH05222041A (ja) * 1992-02-13 1993-08-31 Mitsubishi Gas Chem Co Inc アデニン誘導体の精製法
WO1995020377A1 (en) * 1994-01-27 1995-08-03 The Board Of Regents Of The University Of Oklahoma Rapidly dissolving oral dosage form
US5607697A (en) * 1995-06-07 1997-03-04 Cima Labs, Incorporated Taste masking microparticles for oral dosage forms
EP0993524B1 (en) 1997-06-30 2002-11-20 Beloit Technologies, Inc. Method and apparatus for the high speed application of coating to a traveling paper web
ES2148120T3 (es) 1997-07-08 2002-01-16 Lundbeck & Co As H Metodo para la preparacion de citalopram.
EA002770B1 (ru) 1997-11-11 2002-08-29 Х.Лундбекк А/С Способ получения циталопрама
FR2785538B1 (fr) * 1998-11-06 2004-04-09 Prographarm Laboratoires Comprime a delitement rapide perfectionne
US20020071864A1 (en) * 1999-03-25 2002-06-13 Yuhan Corporation Rapidly disintegrable tablet for oral administration
ITMI991581A1 (it) 1999-06-25 2001-01-15 Lundbeck & Co As H Metodo per la preparazione di citalopram
ITMI991579A1 (it) 1999-06-25 2001-01-15 Lundbeck & Co As H Metodo per la preparazione di citalopram
JP2001226372A (ja) * 1999-12-06 2001-08-21 Sumika Fine Chemicals Co Ltd ロサルタンの結晶性または結晶化された酸付加塩およびロサルタンの精製方法
GB2357762B (en) * 2000-03-13 2002-01-30 Lundbeck & Co As H Crystalline base of citalopram
WO2002030400A1 (fr) * 2000-10-06 2002-04-18 Takeda Chemical Industries, Ltd. Preparations solides
KR20030042006A (ko) * 2000-10-16 2003-05-27 다이이찌 세이야꾸 가부시기가이샤 구강내 속붕괴성 의약 조성물 및 그의 제조방법
US7799342B2 (en) * 2000-12-06 2010-09-21 Wyeth Llc Fast dissolving tablet
WO2001045483A2 (en) * 2000-12-22 2001-06-28 H. Lundbeck A/S Method for the preparation of pure citalopram
JP2003519121A (ja) * 2000-12-28 2003-06-17 ハー・ルンドベック・アクチエゼルスカベット 純粋なシタロプラムの製造方法
WO2002087566A1 (en) * 2001-05-01 2002-11-07 H. Lundbeck A/S The use of enantiomeric pure escitalopram
US6872405B2 (en) * 2001-05-10 2005-03-29 Yamanouchi Pharmaceutical Co., Ltd. Quick-disintegrating tablet in buccal cavity and manufacturing method thereof
GB0113842D0 (en) * 2001-06-07 2001-08-01 Boots Co Plc Therapeutic agents
AR034612A1 (es) * 2001-06-25 2004-03-03 Lundbeck & Co As H Proceso para la preparacion del citalopram racemico y/o del s- o r-citalopram mediante la separacion de una mezcla de r- y s-citalopram
AR034759A1 (es) 2001-07-13 2004-03-17 Lundbeck & Co As H Metodo para la preparacion de escitalopram
IL159326A0 (en) * 2001-07-31 2004-06-01 Lundbeck & Co As H Crystalline composition containing escitalopram
IS7239A (is) 2001-12-14 2004-04-29 H. Lundbeck A/S Aðferð til framleiðslu á essítalóprami
US7148364B2 (en) * 2002-01-07 2006-12-12 Sun Pharmaceutical Industries Process for the preparation of 1-[3-(dimethylamino)propyl]-1-(4-fluorophenyl)-1,3-dihydro-5-isobenzofuran carbonitrile
FR2834889B1 (fr) * 2002-01-18 2004-04-02 Roquette Freres Forme pharmaceutique solide orodispersible
GB0204607D0 (en) * 2002-02-27 2002-04-10 Matrix Lab Ltd Process
EP1517676A1 (en) * 2002-05-03 2005-03-30 Skyepharma Canada Inc. Oral dosage forms comprising fenofibrate
AU2003287919B2 (en) 2002-12-23 2009-11-12 H. Lundbeck A/S Escitalopram hydrobromide and a method for the preparation thereof
CN1510024A (zh) * 2002-12-24 2004-07-07 北京德众万全药物技术开发有限公司 可用于制备西酞普兰(s)-对映异构体的新的化合物及其制备方法
DE10305984A1 (de) * 2003-02-13 2004-09-02 Helm Ag Salze organischer Säuren mit Clopidogrel und deren Verwendung zur Herstellung phamazeutischer Formulierungen
JP4739217B2 (ja) * 2003-05-07 2011-08-03 サムヤン コーポレイション 速く溶ける錠剤を製造するための高可塑性顆粒
US8647668B2 (en) * 2003-10-15 2014-02-11 Fuji Chemical Industry Co., Ltd. Tablet quickly disintegrating in oral cavity
WO2005049596A1 (en) * 2003-11-20 2005-06-02 Natco Pharma Limited A process for the preparation of high purity escitalopram
HU227491B1 (en) * 2003-11-25 2011-07-28 Egis Gyogyszergyar Nyilvanosan Muekoedoe Reszvenytarsasag Tablet containing citalopram hydrogen bromide
WO2005084643A1 (en) * 2004-03-05 2005-09-15 H. Lundbeck A/S Crystalline composition containing escitalopram oxalate
EP1877394A1 (en) * 2005-04-04 2008-01-16 Jubilant Organosys Limited Process for the preparation of escitalopram or its acid addition salts

Also Published As

Publication number Publication date
IL187454A0 (en) 2008-02-09
SG169358A1 (en) 2011-03-30
SK500402007A3 (sk) 2008-05-06
ZA200901698B (en) 2010-04-28
CA2612827C (en) 2010-11-30
GB2448834B (en) 2010-01-20
TR200708792T1 (tr) 2008-05-21
LT2008005A (en) 2008-10-27
FI20077133L (fi) 2007-12-20
AR079750A2 (es) 2012-02-15
TR201000625T1 (tr) 2010-03-22
AT11883U1 (de) 2011-06-15
JP4415056B2 (ja) 2010-02-17
NO20080359L (no) 2008-01-18
DK1896439T4 (da) 2015-01-12
GB2442160A (en) 2008-03-26
AT10983U1 (de) 2010-02-15
CZ2007898A3 (cs) 2008-01-23
KR20100133023A (ko) 2010-12-20
RS51575B2 (sr) 2018-02-28
IS8705A (is) 2008-01-14
FI20080548L (fi) 2008-10-07
GB0811164D0 (en) 2008-07-23
EP2385044A1 (en) 2011-11-09
UA86536C2 (ru) 2009-04-27
EP1896439B2 (en) 2014-10-15
KR101340815B1 (ko) 2013-12-11
WO2006136169A2 (en) 2006-12-28
EP1896439B1 (en) 2011-02-02
BRPI0612295A2 (pt) 2011-01-04
ES2319073B1 (es) 2010-02-26
PL384185A1 (pl) 2008-06-23
MY143239A (en) 2011-04-15
ATE497500T1 (de) 2011-02-15
GB0724557D0 (en) 2008-01-23
JP4906852B2 (ja) 2012-03-28
JP2009046506A (ja) 2009-03-05
EP2325177A1 (en) 2011-05-25
JP2009179635A (ja) 2009-08-13
CA2612827A1 (en) 2006-12-28
TWI358407B (en) 2012-02-21
EA201001108A1 (ru) 2011-02-28
CZ300686B6 (cs) 2009-07-15
JP2008546724A (ja) 2008-12-25
ZA200711066B (en) 2009-07-29
HUP0800135A2 (en) 2008-06-30
EE00773U1 (et) 2008-10-15
SI1896439T2 (sl) 2014-12-31
GB2448834A (en) 2008-10-29
TWI347942B (en) 2011-09-01
AR055062A1 (es) 2007-08-01
DE112006001619T5 (de) 2008-06-12
HRP20110093T4 (hr) 2015-02-27
JP2012072168A (ja) 2012-04-12
AU2006261452A1 (en) 2006-12-28
ES2319073A1 (es) 2009-05-01
FI20080548A7 (fi) 2008-10-07
HUP0800135A3 (en) 2009-01-28
KR20110084341A (ko) 2011-07-21
PL1896439T5 (pl) 2016-01-29
KR20110033310A (ko) 2011-03-30
TW200740785A (en) 2007-11-01
LT5550B (lt) 2009-03-25
EA019239B1 (ru) 2014-02-28
MY143252A (en) 2011-04-15
ES2356838T5 (es) 2015-01-26
GB2442160B (en) 2010-01-20
AU2010200844A1 (en) 2010-04-01
RS51575B (sr) 2011-08-31
DK1896439T3 (da) 2011-02-28
KR20120064140A (ko) 2012-06-18
TW201130808A (en) 2011-09-16
PT1896439E (pt) 2011-02-15
CN101928269A (zh) 2010-12-29
ES2356838T3 (es) 2011-04-13
SI1896439T1 (sl) 2011-03-31
KR20080018191A (ko) 2008-02-27
CY1112392T1 (el) 2015-12-09
HRP20110093T1 (hr) 2011-03-31
EP1896439A2 (en) 2008-03-12
MX2007015328A (es) 2008-02-15
CA2646780A1 (en) 2006-12-28
PL1896439T3 (pl) 2011-04-29
LV13677B (en) 2008-05-20
EA200800102A1 (ru) 2008-04-28
NO20101777L (no) 2008-01-18
BG66086B1 (bg) 2011-03-31
WO2006136169A3 (en) 2007-10-18
CZ299906B6 (cs) 2008-12-29
CZ301286B6 (cs) 2009-12-30
JP5731957B2 (ja) 2015-06-10
DE602006019961D1 (de) 2011-03-17
AU2006261452B2 (en) 2010-02-04
BG110024A (bg) 2008-05-30
CN101189220A (zh) 2008-05-28
DK200800075A (da) 2008-03-15
FI20077133A7 (fi) 2007-12-20
JP2009179634A (ja) 2009-08-13

Similar Documents

Publication Publication Date Title
DK200900284A (da) Krystallinsk base af escitalopram og smeltetabletter indeholdende escitalopram base
JP2010047612A5 (da)
RU2000123156A (ru) Быстро расщепляющаяся фармацевтическая лекарственная форма
UA105203C2 (ru) Твердая фармацевтическая композиция, которая содержит амлодипин и лозартан
RU2017133990A (ru) Фармацевтические лекарственные формы ингибитора тирозинкиназы брутона
WO2007052289A3 (en) Novel dispersible tablet composition
JP2011037832A5 (da)
RU2012106139A (ru) Лекарственные формы цитрата железа (iii)
WO2003086362A3 (en) Method of stabilizing bupropion hydrochloride tablets
NO20074480L (no) Hurtig massefuktingsmetode for fremstilling av kalsium-inneholdende sammensetninger
JP2022116267A (ja) トホグリフロジンを含有する固形製剤及びその製造方法
RU2011112362A (ru) Твердые препаративные формы оспемифена
RU2008135718A (ru) Композиции клопидогреля бисульфата
FI3769765T3 (fi) Natriumalkyylisulfaattia sisältävä farmaseuttinen koostumus
NO20024237L (no) Farmasöytiske formuleringer
HRP20130108T1 (hr) Farmaceutski sastav koji sadrži aleglitazar
WO2009135950A3 (en) Process for preparing a tablet containing excipients
SI1773292T1 (sl) Hitro razgradljiva oralno disperzibilna farmacevtska oblika
RU2012121183A (ru) Фармацевтическая композиция для перорального введения
FI3993777T3 (fi) Kompressoidut masitentaanikoostumukset, menetelmät ja niiden käytöt
RU2014145845A (ru) Таблетка с замедленным высвобождением, содержащая леводропропизин и способ ее изготовлеия
ATE462414T1 (de) Irbesartan enthaltende feste zubereitung
JP2017520628A5 (da)
WO2005034954A3 (en) Pharmaceutical compositions of paroxetine containing microcrystalline cellulose, prepared by wet granulation
JP2018127416A (ja) フェブキソスタット含有錠剤の製造方法

Legal Events

Date Code Title Description
ATS Application withdrawn