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Inventor:
Woog; Heinrich
Address:
Laudenbach, DE
No. of patents:
18
Patents:




Patent Number Title Of Patent Date Issued
6689755 Method of stabilizing biologically active substances February 10, 2004
The present invention relates to a rapid and readily reproducible process for stabilizing biologically active substances by combining the biologically active substance witha a stabilizingmixture and drying the resulting mixture into a dry, amorphous product by means of convection dry
6664284 Stabilized carvedilol injection solution December 16, 2003
Ready-to-use, aqueous injection solutions containing carvedilol (1-(9H-carbazolyl-4-yloxy)-3-[[(2-(2-methoxyphenoxy)ethyl]-amino]-2-propan ol) or its pharmacologically harmless salts which are stable in storage and are well tolerated by veins are disclosed.
6627221 Pharmaceutical composition containing diphosphonic acid or salt thereof September 30, 2003
The invention relates to a solid pharmaceutical form of administration containing a diphosphonic acid or a physiologically compatible salt thereof as the active substance, wherein the active substance is present in granulate form, optionally together with pharmaceutical adjuvants in
6521262 Solid instant-release forms of administration and process for producing the same February 18, 2003
The present invention concerns solid instant-release forms of administration (IR form of administration) comprising therapeutic active substances or active substance concentrates in particular lipid conjugates of nucleosides which have gel-forming properties in aqueous media as well
6419955 Process for making bisphosphonate compositions July 16, 2002
The present invention relates to a process for the preparation of bisphonate-containing pharmaceutical compositions for oral administration wherein the active substance is wet-granulated in a fluidized-bed granulator and the wet granulate is dried in the fluidised bed granulator. The
6303113 Process for the production of pharmaceutical preparations containing human protein for infusion October 16, 2001
The present invention concerns a process for the production of well-tolerated, preserved injection or infusion solutions containing human protein.
6294196 Pharmaceutical composition containing diphosphonic acid or salt thereof September 25, 2001
The invention relates to a solid pharmaceutical form of administration containing a diphosphonic acid or a physiologically compatible salt thereof as the active substance, wherein the active substance is present in granulate form, optionally together with pharmaceutical adjuvants in
6143326 Oral pharmaceutical preparation containing ibandronat November 7, 2000
The invention is directed to well-tolerated pharmaceutical compositions for oral application, containing ibandronate or a physiologically tolerable salt thereof as active substance, the administration form consisting of an active substance-containing inner portion enclosed in such fashio
5919757 Aqueous pharmaceutical preparations of G-CSF with a long shelf life July 6, 1999
Aqueous pharmaceutical preparations of G-CSF are disclosed that are stable on storage and a buffer selected from the group consisting of a salt of citrate, maleate, a combination of phosphate and citrate, and arginine; and at least one surfactant.
5919443 Stable lyophilized pharmaceutical preparations of G-CSF July 6, 1999
The present invention concerns lyophilized pharmaceutical preparations of G-CSF that contain maltose, raffinose, sucrose, trehalose or amino sugar as stabilizing agents. In additon the invention concerns a process for the production of stabilized lyophilisates as well as the use of malto
5747030 Pharmaceutical preparation containing plasminogen activators May 5, 1998
The invention relates to pharmaceutical preparations containing plasminogen activators, sugars and tranexamic acid, in the form of a lyophilisate or an injection or infusion solution. In particular, the preparations contain a sugar, phosphate buffer, tranexamic acid as well as a surfacta
5662918 Pharmaceutical agents containing diphosphonic acids and salts thereof September 2, 1997
The invention concerns pharmaceutical preparations that are stable on storage, which contain at least one diphosphonic acid and/or at least one physiologically acceptable salt of such an acid as the active substance.
5504099 Injection solutions of azosemide which are ready for injection April 2, 1996
Aqueous injection solution that is ready-for-injection of a water-soluble, physiologically well-tolerated azosemide salt of an organic amide, which contains an organic solvent and if desired, a physiologically well-tolerated buffer and it concerns a process for the production of such
5503827 Process for the production of multi-dose pharmaceutical preparations containing isolated or reco April 2, 1996
The present invention concerns a process for the production of well-tolerated, preserved injection or infusion solutions containing human protein.
5324749 Pharmaceutical aqueous solution of 4-[2-(benzene-sulphonylamino)-ethyl]-phenoxyacetic acid June 28, 1994
The present invention concerns a storage-stable, aqueous solution of 4-[2-(benzenesulphonylamino)-ethyl]-phenoxyacetic acid for pharmaceutical purposes.
4992419 Stabilized erythropoietin preparations February 12, 1991
A compatible, storage-stable human protein preparation containing a human protein, a physiologically compatible buffer and optionally complex formers, isotonia-adjusting agents, calcium chloride and other materials usual for injection purposes which, in an injectable form, contains 5 to
4861786 Composition for a stable vein compatible injectable solution of torasemide process for the prepa August 29, 1989
The present invention provides an aqueous, alkaline injection solution of torasemide ready for injection, which contains a physiologically compatible alkaline buffer with a pH value of from 9.3 to 9.9 and with a buffer capacity of up to 0.1 val/liter together with an organic solvent in
4191772 Instillation composition March 4, 1980
An instillation composition, comprising an effective amount of at least one sparingly soluble active material suspended or partly dissolved in an aqueous emulsion containing a swelling agent. Advantageously the active substance is nitrofurantoin or a quinolone or pyridazine derivative, t


 
 
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