UY26318A1 - Formas de administracion oral con liberacion total controlada de sustancia activa, encontrandose una misma sustancia activa en forma de al menos dos sales distintas que en la forma de administracion se encuentran en estado solido y que presentan dife - Google Patents

Formas de administracion oral con liberacion total controlada de sustancia activa, encontrandose una misma sustancia activa en forma de al menos dos sales distintas que en la forma de administracion se encuentran en estado solido y que presentan dife

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Publication number
UY26318A1
UY26318A1 UY26318A UY26318A UY26318A1 UY 26318 A1 UY26318 A1 UY 26318A1 UY 26318 A UY26318 A UY 26318A UY 26318 A UY26318 A UY 26318A UY 26318 A1 UY26318 A1 UY 26318A1
Authority
UY
Uruguay
Prior art keywords
active substance
solid state
oral administration
controlled release
dife
Prior art date
Application number
UY26318A
Other languages
English (en)
Inventor
Johannes Bartholomaus Ziegler
Original Assignee
Gruenenthal Chemie
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
Priority claimed from DE19940740A external-priority patent/DE19940740A1/de
Priority claimed from DE19940944A external-priority patent/DE19940944B4/de
Priority claimed from DE10023699A external-priority patent/DE10023699A1/de
Application filed by Gruenenthal Chemie filed Critical Gruenenthal Chemie
Publication of UY26318A1 publication Critical patent/UY26318A1/es

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    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D275/00—Heterocyclic compounds containing 1,2-thiazole or hydrogenated 1,2-thiazole rings
    • C07D275/04—Heterocyclic compounds containing 1,2-thiazole or hydrogenated 1,2-thiazole rings condensed with carbocyclic rings or ring systems
    • C07D275/06—Heterocyclic compounds containing 1,2-thiazole or hydrogenated 1,2-thiazole rings condensed with carbocyclic rings or ring systems with hetero atoms directly attached to the ring sulfur atom
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    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C217/00—Compounds containing amino and etherified hydroxy groups bound to the same carbon skeleton
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    • C07C217/74—Compounds containing amino and etherified hydroxy groups bound to the same carbon skeleton having etherified hydroxy groups bound to carbon atoms of at least one six-membered aromatic ring and amino groups bound to acyclic carbon atoms or to carbon atoms of rings other than six-membered aromatic rings of the same carbon skeleton with rings other than six-membered aromatic rings being part of the carbon skeleton
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    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C307/00—Amides of sulfuric acids, i.e. compounds having singly-bound oxygen atoms of sulfate groups replaced by nitrogen atoms, not being part of nitro or nitroso groups
    • C07C307/02—Monoamides of sulfuric acids or esters thereof, e.g. sulfamic acids
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    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D291/00—Heterocyclic compounds containing rings having nitrogen, oxygen and sulfur atoms as the only ring hetero atoms
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    • A61K9/0053—Mouth and digestive tract, i.e. intraoral and peroral administration
    • A61K9/0056—Mouth soluble or dispersible forms; Suckable, eatable, chewable coherent forms; Forms rapidly disintegrating in the mouth; Lozenges; Lollipops; Bite capsules; Baked products; Baits or other oral forms for animals
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    • A61K9/0095—Drinks; Beverages; Syrups; Compositions for reconstitution thereof, e.g. powders or tablets to be dispersed in a glass of water; Veterinary drenches
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
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    • C07C2601/12—Systems containing only non-condensed rings with a six-membered ring
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Abstract

La invención se refiere a formas de administración oral con liberación total controlada de sustancia activa, encontrándose una misma sustancia activa en forma de al menos dos sales distintas que en la forma de administración se encuentran en estado sólido y que presentan diferente liberación in vitro de la sustancia activa
UY26318A 1999-08-31 2000-08-31 Formas de administracion oral con liberacion total controlada de sustancia activa, encontrandose una misma sustancia activa en forma de al menos dos sales distintas que en la forma de administracion se encuentran en estado solido y que presentan dife UY26318A1 (es)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
DE19940740A DE19940740A1 (de) 1999-08-31 1999-08-31 Pharmazeutische Salze
DE19940944A DE19940944B4 (de) 1999-08-31 1999-08-31 Retardierte, orale, pharmazeutische Darreichungsformen
DE10023699A DE10023699A1 (de) 1999-08-31 2000-05-16 Retardierte Darreichungsform enthaltend Tramadolsaccharinat

Publications (1)

Publication Number Publication Date
UY26318A1 true UY26318A1 (es) 2000-10-31

Family

ID=27213855

Family Applications (2)

Application Number Title Priority Date Filing Date
UY26321A UY26321A1 (es) 1999-08-31 2000-08-31 Formas de administracion de tramadol retardadas mediante un revestimiento que contiene la sustancia activa tramadol en forma de sacarinato de tramadol asi como eventualmente otros excipientes
UY26318A UY26318A1 (es) 1999-08-31 2000-08-31 Formas de administracion oral con liberacion total controlada de sustancia activa, encontrandose una misma sustancia activa en forma de al menos dos sales distintas que en la forma de administracion se encuentran en estado solido y que presentan dife

Family Applications Before (1)

Application Number Title Priority Date Filing Date
UY26321A UY26321A1 (es) 1999-08-31 2000-08-31 Formas de administracion de tramadol retardadas mediante un revestimiento que contiene la sustancia activa tramadol en forma de sacarinato de tramadol asi como eventualmente otros excipientes

Country Status (21)

Country Link
US (2) US6576260B2 (es)
EP (2) EP1207866B1 (es)
JP (2) JP2003508430A (es)
CN (2) CN1202815C (es)
AT (1) ATE279186T1 (es)
AU (2) AU781058B2 (es)
BR (2) BR0013825A (es)
CA (2) CA2388560A1 (es)
CZ (2) CZ2002671A3 (es)
ES (1) ES2226886T3 (es)
HK (1) HK1047230B (es)
HU (2) HUP0203623A2 (es)
IL (2) IL148411A0 (es)
MX (2) MXPA02002193A (es)
NO (2) NO20020939L (es)
NZ (2) NZ517559A (es)
PL (2) PL354264A1 (es)
PT (1) PT1207866E (es)
SK (2) SK2762002A3 (es)
UY (2) UY26321A1 (es)
WO (2) WO2001015683A1 (es)

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DE19940740A1 (de) * 1999-08-31 2001-03-01 Gruenenthal Gmbh Pharmazeutische Salze
DE60107393T2 (de) 2000-03-01 2005-12-01 Euro-Celtique S.A. Verwendung von tramadol zur herstellung eines arzneimittels zur behandlung von funktionelle gastrointestinale krankenheiten
DE10013029A1 (de) * 2000-03-17 2001-09-20 Roehm Gmbh Mehrschichtige Arzneiform für die Colonfreigabe
DE10108122A1 (de) * 2001-02-21 2002-10-02 Gruenenthal Gmbh Arzneimittel auf Basis von Tramadol
DE10109763A1 (de) * 2001-02-28 2002-09-05 Gruenenthal Gmbh Pharmazeutische Salze
US20050176790A1 (en) 2001-02-28 2005-08-11 Johannes Bartholomaus Pharmaceutical salts
DE10141650C1 (de) 2001-08-24 2002-11-28 Lohmann Therapie Syst Lts Transdermales Therapeutisches System mit Fentanyl bzw. verwandten Substanzen
US8101209B2 (en) 2001-10-09 2012-01-24 Flamel Technologies Microparticulate oral galenical form for the delayed and controlled release of pharmaceutical active principles
US20050182056A9 (en) * 2002-02-21 2005-08-18 Seth Pawan Modified release formulations of at least one form of tramadol
US8128957B1 (en) 2002-02-21 2012-03-06 Valeant International (Barbados) Srl Modified release compositions of at least one form of tramadol
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