http://rdf.ncbi.nlm.nih.gov/pubchem/patent/ES-2879675-T3

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filingDate 2017-09-29-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2021-11-22-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_e6b3eb3561524efa2868aa46dba62783
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publicationDate 2021-11-22-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber ES-2879675-T3
titleOfInvention Pharmaceutical composition of 5-HT6 antagonist
abstract An immediate release pharmaceutical composition, which over a total of 100% by weight comprises: a) from 2% to 60% of 1-[(2-bromophenyl)sulfonyl]-5-methoxy-3-[(4-methyl- 1-piperazinyl)methyl]-1H-indole or a pharmaceutically acceptable salt thereof; b) from 36% to 97% diluent or a total of two diluents; wherein the diluent is selected from the group consisting of microcrystalline cellulose, lactose monohydrate, dibasic calcium phosphate, lactose, lactose hydrate, lactose anhydrate, mannitol, starch, and isomaltol; c) from 0.5% to 2% of lubricant; wherein the lubricant is magnesium stearate; d) from 0.5% to 1% slip agent; wherein the slip agent is colloidal silicon dioxide; e) 0% to 10% binder; wherein the binder is selected from the group consisting of povidone or hydroxypropyl methylcellulose; f) 0% to 5% disintegrating agent; wherein the disintegrating agent is selected from crospovidone, sodium starch glycolate and croscarmellose sodium; and g) 0% to 2% acidifying agent; wherein the acidifying agent is citric acid.
priorityDate 2016-10-03-04:00^^<http://www.w3.org/2001/XMLSchema#date>
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