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<title><![CDATA[KARYA TULIS ILMIAH UJI MUTU FISIK TABLET METOCLOPRAMIDE HCl TERHADAP VARIASI LAMA PROSES PENCAMPURAN FASE LUAR DENGAN METODE GRANULASI BASAH]]></title>
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<namePart>Chofifa</namePart>
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<namePart>Apt. Deny Budi Legowo, S.Farm., M.Farm</namePart>
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<namePart>Dr. Iswandi, S.Si, M.Farm., Apt</namePart>
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<name type="Personal Name">
<namePart>Apt. Valiandri Puspadina, S.Farm</namePart>
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<name type="Personal Name">
<namePart>Apt. Deny Budi Legowo, S.Farm., M.Farm</namePart>
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<place><placeTerm type="text"><![CDATA[Krian]]></placeTerm></place>
<publisher><![CDATA[Akademi Farmasi Mitra Sehat Mandiri Sidoarjo]]></publisher>
<dateIssued><![CDATA[2020]]></dateIssued>
<issuance><![CDATA[monographic]]></issuance>
<edition><![CDATA[Published]]></edition>
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<languageTerm type="text"><![CDATA[Indonesia]]></languageTerm>
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<itemTypeTerm type="text"><![CDATA[KARYA TULIS ILMIAH]]></itemTypeTerm>
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<note>Metoclopramide HCl is used to relieve nausea and vomiting. Continuous nausea  and  vomiting  may  result  in  a  harmful  electrolyte  disturbance,  resulting in  a  medication  that  is  formulated  in  a  tablet  that  is  expected  to  relieve  nausea and vomiting.Metoclopramide HCl tablet preparations were made by using variations in the length of the external phase mixing process that is 5 minutes, 10 minutes, and 15  minutes.  Tablet  preparations  are  made  using  wet  granulation.Data  collection was  carried  out  by  covering  physical  characteristics  including  oraganoleptic, uniformity  in  weight,  uniformity  in  size,  hardness  of  tablets,  fragility  of  tablets, disintegration  time  of  tablets,  dissolution  test  and  levels  of  metoclopramide  HCl. Physical  quality  test  results  were  statistically  analyzed  to  determine  the  effect  of the mixing process duration on the characteristics of tablets.The  results  showed  that  the  preparation  of  metoclopramide  tablets  was 0.31mm thickness, 0.133-0.135mg tablet weight variation, 3-4Kp tablet hardness, 4.29-5.63%   tablet   fragility,   tablet   crushing   time   1,53-5,13   minutes,   content uniformity  of  101.04-106.36%,  and  dissolution  of  69.31-100.15%.  The  results obtained the longer the process of mixingthe outer phase, the greater the elasticity of the tablet.</note>
<subject authority=""><topic><![CDATA[Tablet]]></topic></subject>
<subject authority=""><topic><![CDATA[Metoklopramide HCl]]></topic></subject>
<subject authority=""><topic><![CDATA[uji mutu fisik]]></topic></subject>
<subject authority=""><topic><![CDATA[Spektrofotometri UV-Vis]]></topic></subject>
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