Abstract: Non-deliquescent formulation comprising or consisting of sodium valproate and cyclodextrin having a molar ratio of sodium valproate to cyclodextrin within the range of from 1:0.01 to 1:0.09.
Abstract: A transdermal patch contains an active loratidine metabolite contained with a polyacrylate polymer matrix. The transdermal patch provides pharmaceutically useful transdermal flux rates over time.
Type:
Grant
Filed:
March 23, 1998
Date of Patent:
December 26, 2000
Assignee:
Hexal AG
Inventors:
Karin Klokkers, Wilfried Fischer, Daniel Bracher
Abstract: The object of the present invention is an oral drug preparation containing the .gamma.-cyclodextrin complex of diclofenac or pharmaceutically acceptable salts thereof, especially the sodium salt prepared by known methods, and by which the gastro-intestinal irritancy of diclofenac, at the same or improved bioavailability, can be considerably decreased.
Abstract: The invention relates to a pharmaceutical composition consisting of or containing cyclosporin A and .alpha.-tocopherol or one of the derivatives thereof.
Abstract: The invention relates to a transdermal therapeutic system (TTS) for the administration of active agents for substitution treatment of drug dependency or drug addiction.
Abstract: The invention relates to a tablet or capsule that is characterised by a powder mixture having a content of stable ranitidine hydrochloride Form 1 together with a carrier and/or diluent, and to manufacturing processes for the tablet.
Abstract: A transdermal system in the form of a patch that comprises a tamoxifen derivative and an absorption-promoting additive for systemic administration.
Type:
Grant
Filed:
September 5, 1997
Date of Patent:
May 18, 1999
Assignee:
Hexal AG
Inventors:
Wilfried Fischer, Karin Klokkers, Anna Sendl-Lang
Abstract: The invention relates to a sustained release tablet containing diclofenac-Na as active material and methylhydroxypropylcellulose as sustained release agent.
Abstract: Thyroxine containing pharmaceutical compositions with improved aqueous solubility, stability and enhanced membrane permeation have been prepared by formulating thyroxine with cyclodextrins. These thyroxine/cyclodextrin complexes can further be transformed into different dosage forms (oral tablets, injectables, transdermal patches, hydrogels, ointments, suppositories etc.) by employing known, common pharmaceutical additives.