echemi logo
Product
  • Product
  • Supplier
  • Inquiry
    Home > Medical News > Medical Research Articles > Over 1 billion oral hypoglycemic drugs!

    Over 1 billion oral hypoglycemic drugs!

    • Last Update: 2022-05-14
    • Source: Internet
    • Author: User
    Search more information of high quality chemicals, good prices and reliable suppliers, visit www.echemi.com
    A few days ago, the official website of the State Food and Drug Administration showed that Chengdu Hengrui Pharmaceutical's Gliclazide sustained-release tablets and Jiangxi Pharmaceutical (a subsidiary of Renhe Pharmaceutical)'s Gliclazide sustained-release tablets were both approved as supplementary applications
    .
    The latest data from Minet shows that in 2021, the sales of Gliclazide sustained-release tablets in public medical institutions in China will be nearly 1.
    2 billion yuan, of which Servier has the largest market share
    .
     
    The data show that Gliclazide extended-release tablets are mainly used for non-islet-dependent diabetes mellitus when dietary therapy alone is insufficient to control blood sugar, and its blood sugar lowering intensity is between tolbutamide and excellent blood sugar
    .
     
    The latest data from Minet.
    com shows that in 2021, the sales of terminal Gliclazide sustained-release tablets in China's urban public hospitals, county-level public hospitals, urban community centers and township health centers (referred to as Chinese public medical institutions) will be nearly 1.
    2 billion yuan.
    Via has the largest market share, accounting for more than 50%
    .
     
    At present, 22 companies have the production approval for Gliclazide sustained-release tablets, of which 8 companies including Chengdu Hengrui Pharmaceutical, Jiangxi Pharmaceutical, Yichang Renfu Pharmaceutical, Shandong Lukang Pharmaceutical Group Saite have been approved with supplementary applications comment
    .
     
    In addition, 3 companies including China Resources Shuanghe Limin Pharmaceutical (Jinan) and Ningbo Keercom Minovar Pharmaceutical submitted their marketing applications under the category 4 imitations.
    The supplementary application for sexuality evaluation is under review and approval
    .
     
    Source: State Food and Drug Administration official website, Minet database
    A few days ago, the official website of the State Food and Drug Administration showed that Chengdu Hengrui Pharmaceutical's Gliclazide sustained-release tablets and Jiangxi Pharmaceutical (a subsidiary of Renhe Pharmaceutical)'s Gliclazide sustained-release tablets were both approved as supplementary applications
    .
    The latest data from Minet shows that in 2021, the sales of Gliclazide sustained-release tablets in public medical institutions in China will be nearly 1.
    2 billion yuan, of which Servier has the largest market share
    .
     
    The data show that Gliclazide extended-release tablets are mainly used for non-islet-dependent diabetes mellitus when dietary therapy alone is insufficient to control blood sugar, and its blood sugar lowering intensity is between tolbutamide and excellent blood sugar
    .
     
    The latest data from Minet.
    com shows that in 2021, the sales of terminal Gliclazide sustained-release tablets in China's urban public hospitals, county-level public hospitals, urban community centers and township health centers (referred to as Chinese public medical institutions) will be nearly 1.
    2 billion yuan.
    Via has the largest market share, accounting for more than 50%
    .
     
    At present, 22 companies have the production approval for Gliclazide sustained-release tablets, of which 8 companies including Chengdu Hengrui Pharmaceutical, Jiangxi Pharmaceutical, Yichang Renfu Pharmaceutical, Shandong Lukang Pharmaceutical Group Saite have been approved with supplementary applications comment
    .
     
    In addition, 3 companies including China Resources Shuanghe Limin Pharmaceutical (Jinan) and Ningbo Keercom Minovar Pharmaceutical submitted their marketing applications under the category 4 imitations.
    The supplementary application for sexuality evaluation is under review and approval
    .
     
    Source: State Food and Drug Administration official website, Minet database
    A few days ago, the official website of the State Food and Drug Administration showed that Chengdu Hengrui Pharmaceutical's Gliclazide sustained-release tablets and Jiangxi Pharmaceutical (a subsidiary of Renhe Pharmaceutical)'s Gliclazide sustained-release tablets were both approved as supplementary applications
    .
    The latest data from Minet shows that in 2021, the sales of Gliclazide sustained-release tablets in public medical institutions in China will be nearly 1.
    2 billion yuan, of which Servier has the largest market share
    .
     
    The data show that Gliclazide extended-release tablets are mainly used for non-islet-dependent diabetes mellitus when dietary therapy alone is insufficient to control blood sugar, and its blood sugar lowering intensity is between tolbutamide and excellent blood sugar
    .
     
    The latest data from Minet.
    com shows that in 2021, the sales of terminal Gliclazide sustained-release tablets in China's urban public hospitals, county-level public hospitals, urban community centers and township health centers (referred to as Chinese public medical institutions) will be nearly 1.
    2 billion yuan.
    Via has the largest market share, accounting for more than 50%
    .
     
    At present, 22 companies have the production approval for Gliclazide sustained-release tablets, of which 8 companies including Chengdu Hengrui Pharmaceutical, Jiangxi Pharmaceutical, Yichang Renfu Pharmaceutical, Shandong Lukang Pharmaceutical Group Saite have been approved with supplementary applications comment
    .
     
    In addition, 3 companies including China Resources Shuanghe Limin Pharmaceutical (Jinan) and Ningbo Keercom Minovar Pharmaceutical submitted their marketing applications under the category 4 imitations.
    The supplementary application for sexuality evaluation is under review and approval
    .
     
    Source: State Food and Drug Administration official website, Minet database
    This article is an English version of an article which is originally in the Chinese language on echemi.com and is provided for information purposes only. This website makes no representation or warranty of any kind, either expressed or implied, as to the accuracy, completeness ownership or reliability of the article or any translations thereof. If you have any concerns or complaints relating to the article, please send an email, providing a detailed description of the concern or complaint, to service@echemi.com. A staff member will contact you within 5 working days. Once verified, infringing content will be removed immediately.

    Contact Us

    The source of this page with content of products and services is from Internet, which doesn't represent ECHEMI's opinion. If you have any queries, please write to service@echemi.com. It will be replied within 5 days.

    Moreover, if you find any instances of plagiarism from the page, please send email to service@echemi.com with relevant evidence.