01 1Fujian Nanping Qingsong Chemical Co., Ltd.
02 1Nippon Seika Co., Ltd.
03 1Suzhou Youhe Technology Co., Ltd.
04 1Wuzhou Huangpu Chemical Industry Co., Ltd.
01 1Japanese Pharmacopoeia d- camphor
02 2Japanese Pharmacopoeia dl- camphor
03 1Japanese Pharmacopoeia dl- camphor (production only)
01 3China
02 1Japan
Japanese Pharmacopoeia dl-Camphor
Registration Number : 225MF10027
Registrant's Address : No. 85, Taqian Road, Huiyao Industrial Park, Jianyang District, Nanping City, Fujian ...
Initial Date of Registration : 2013-02-13
Latest Date of Registration : 2013-02-13
Japanese Pharmacopoeia d-Camphor
Registration Number : 217MF10184
Registrant's Address : 2-4-9 Bingomachi, Chuo-ku, Osaka City, Osaka Prefecture
Initial Date of Registration : 2005-06-06
Latest Date of Registration : 2006-10-20
Japanese Pharmacopoeia DL-Camphor
Registration Number : 224MF10085
Registrant's Address : Dongsha, Nanfeng Town, Zhangjiagang City, Jiangsu Province
Initial Date of Registration : 2012-04-13
Latest Date of Registration : 2012-04-13
Japanese Pharmacopoeia dl-Camphor (For manufacturing purposes only)
Registration Number : 228MF10069
Registrant's Address : No.1 Wusong Road, Wanxiu District, Wuzhou City
Initial Date of Registration : 2016-02-29
Latest Date of Registration : 2016-02-29
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PharmaCompass offers a list of Camphor 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 Camphor manufacturer or Camphor supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Camphor manufacturer or Camphor supplier.
PharmaCompass also assists you with knowing the Camphor API Price utilized in the formulation of products. Camphor API Price is not always fixed or binding as the Camphor Price is obtained through a variety of data sources. The Camphor Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A 0-07-00-00135 (Beilstein Handbook Reference) manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of 0-07-00-00135 (Beilstein Handbook Reference), including repackagers and relabelers. The FDA regulates 0-07-00-00135 (Beilstein Handbook Reference) manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. 0-07-00-00135 (Beilstein Handbook Reference) API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
click here to find a list of 0-07-00-00135 (Beilstein Handbook Reference) manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A 0-07-00-00135 (Beilstein Handbook Reference) supplier is an individual or a company that provides 0-07-00-00135 (Beilstein Handbook Reference) active pharmaceutical ingredient (API) or 0-07-00-00135 (Beilstein Handbook Reference) finished formulations upon request. The 0-07-00-00135 (Beilstein Handbook Reference) suppliers may include 0-07-00-00135 (Beilstein Handbook Reference) API manufacturers, exporters, distributors and traders.
click here to find a list of 0-07-00-00135 (Beilstein Handbook Reference) suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
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 0-07-00-00135 (Beilstein Handbook Reference) Drug Master File in Japan (0-07-00-00135 (Beilstein Handbook Reference) JDMF) empowers 0-07-00-00135 (Beilstein Handbook Reference) 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 0-07-00-00135 (Beilstein Handbook Reference) JDMF during the approval evaluation for pharmaceutical products. At the time of 0-07-00-00135 (Beilstein Handbook Reference) JDMF registration, PMDA checks if the format is accurate, if the necessary items have been included (application), and if data has been attached.
click here to find a list of 0-07-00-00135 (Beilstein Handbook Reference) suppliers with JDMF on PharmaCompass.
We have 4 companies offering 0-07-00-00135 (Beilstein Handbook Reference)
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