http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-0998272-A1

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filingDate 1998-07-21-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_71a9ab9eb0dc5ebba9d63c770c43a2d1
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_1b1395ef595f4b4a43e754bcd50d6892
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_b94eb4083570c846d2f32561712661e4
publicationDate 2000-05-10-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber EP-0998272-A1
titleOfInvention Pharmaceutical composition for combination of piperidinoalkanol-decongestant
abstract The present invention provides a pharmaceutical composition in the form of a bilayer tablet comprising: (a) a first discrete zone made with Formulation (A) which comprises a therapeutically effective decongestant amount of a sympathomimetic drug, or a pharmaceutically acceptable salt thereof, in an amount of about 18 % to about 39 % by weight of Formulation (A), and a first carrier base material, the first carrier base material comprising a mixture of: (i) carnauba wax in an amount of about 59 % to about 81 % by weight of Formulation (A); and (ii) a suitable antiadherent in an amount of about 0.25 % to about 2.00 % by weight of Formulation (A); wherein said first carrier base material provides a sustained release of the sympathomimetic drug; and (b) a second discrete zone made with Formulation (B) which comprises a therapeutically effective antihistaminic amount of a piperidinoalkanol, or a pharmaceutically acceptable salt thereof, in an amount of about 15 % to about 30 % by weight of Formulation (B) and a second carrier base material, the second carrier base comprisisng a mixture of: (i) a cellulose diluent in an amount of about 27 % to about 73 % by weight of Formulation (B); (ii) pregelatinized starch in an amount of about 15 % to about 30 % by weight of Formulation (B); (iii) a suitable disintegrant in an amount of about 0.25 % to about 6.00 % by weight of Formulation (B); and (iv) a suitable lubricant in an amount of about 0.25 % to about 2.00 % by weight of Formulation (B); wherein said second carrier base material provides an immediate release of the piperidinoalkanol or the pharmaceutically acceptable salt thereof.
priorityDate 1997-08-26-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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