01 2Jiangsu Baozong & Baoda Pharmachem Co. , Ltd.
02 2LIANYUNGANG LONGZHU CHEMICAL CO. , LTD.
03 1SHANGHAI BAOZONG PHARMACEUTICAL CO. , LTD.
04 1WUXI KAILI PHARMACEUTICAL CO. , LTD.
05 1Yancheng Kaili Pharmaceutical Co. , Ltd.
06 1Yatsushiro Pharmaceutical Co., Ltd.
01 2CIMETIDINE
02 2Cimetidine
03 1Cimetidine HP
04 3Day stations cimetidine (production only)
01 5China
02 3Blank
JP Cimetidine (for manufacturing purposes only)
Registration Number : 218MF10648
Registrant's Address : No. 7690 Hutai Road, Luodian Town, Baoshan District, Shanghai, China
Initial Date of Registration : 2006-07-20
Latest Date of Registration : 2009-04-22
Registration Number : 228MF10077
Registrant's Address : No. 10 Yuejiang Road, Rugao Port Fine Chemical Industrial Park, Jiangsu,P. R. China
Initial Date of Registration : 2016-03-29
Latest Date of Registration : 2016-03-29
JP Cimetidine (for manufacturing purposes only)
Registration Number : 223MF10175
Registrant's Address : No. 10 Yuejiang Road, Rugao Port Fine Chemical Industrial Park, Jiangsu,P. R. China
Initial Date of Registration : 2011-12-27
Latest Date of Registration : 2011-12-27
Registration Number : 229MF10111
Registrant's Address : The North side of No. 2 Road, Coastal Industrial Park, Binhai, YanCheng, JiangSu Prov...
Initial Date of Registration : 2017-06-26
Latest Date of Registration : 2017-06-26
Registration Number : 217MF10539
Registrant's Address : Zhoutie Town, Yixing City, Jiangsu Province, P. R. of China
Initial Date of Registration : 2005-09-09
Latest Date of Registration : 2007-09-18
Registration Number : 218MF10246
Registrant's Address : 10-2 Yoshida Shimojima, Higashiosaka City, Osaka Prefecture
Initial Date of Registration : 2006-02-16
Latest Date of Registration : 2010-03-09
Registration Number : 217MF10540
Registrant's Address : INDUSTRIAL ZONE OF CHENGXI TOWN, GANYU COUNTY, LIANYUNGANG, CHINA
Initial Date of Registration : 2005-09-09
Latest Date of Registration : 2007-09-18
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
JP Cimetidine (for manufacturing purposes only)
Registration Number : 219MF10381
Registrant's Address : INDUSTRIAL ZONE OF CHENGXI TOWN, GANYU COUNTY, LIANYUNGANG, CHINA
Initial Date of Registration : 2007-12-19
Latest Date of Registration : 2007-12-19
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
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PharmaCompass offers a list of Cimetidine API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, Price,and more, enabling you to easily find the right Cimetidine manufacturer or Cimetidine supplier for your needs.
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PharmaCompass also assists you with knowing the Cimetidine API Price utilized in the formulation of products. Cimetidine API Price is not always fixed or binding as the Cimetidine Price is obtained through a variety of data sources. The Cimetidine Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Tagamet Hb manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Tagamet Hb, including repackagers and relabelers. The FDA regulates Tagamet Hb manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Tagamet Hb API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
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A Tagamet Hb supplier is an individual or a company that provides Tagamet Hb active pharmaceutical ingredient (API) or Tagamet Hb finished formulations upon request. The Tagamet Hb suppliers may include Tagamet Hb API manufacturers, exporters, distributors and traders.
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The Pharmaceuticals and Medical Devices Agency (PMDA) established the Japan Drug Master File (JDMF), also known as the Master File (MF), to permit Japanese and foreign manufacturers of drug substances, intermediates, excipients, raw materials, and packaging materials (‘Products’) to voluntarily register confidential information about the production and management of their products in Japan.
The Tagamet Hb Drug Master File in Japan (Tagamet Hb JDMF) empowers Tagamet Hb API manufacturers to present comprehensive information (e.g., production methods, data, etc.) to the review authority, i.e., PMDA (Pharmaceuticals & Medical Devices Agency).
PMDA reviews the Tagamet Hb JDMF during the approval evaluation for pharmaceutical products. At the time of Tagamet Hb JDMF registration, PMDA checks if the format is accurate, if the necessary items have been included (application), and if data has been attached.
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We have 4 companies offering Tagamet Hb
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