01 1Sumitomo Chemical Co., Ltd.
02 1Syn-Tech Chem. & Pharm. Co. , Ltd.
01 1Crotamiton
02 1Japan Pharmaceutical Codex crotamiton
01 1Japan
02 1Taiwan
Japanese Pharmacopoeia Non-Drug Standards Crotamiton
Registration Number : 217MF10075
Registrant's Address : 2-7-1 Nihonbashi, Chuo-ku, Tokyo
Initial Date of Registration : 2005-05-23
Latest Date of Registration : 2021-12-09
Registration Number : 228MF10116
Registrant's Address : No. 168 Kai-Yuan Rd. , Hsin-Ying Tainan City, 73055. Taiwan
Initial Date of Registration : 2016-06-21
Latest Date of Registration : 2016-06-21
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PharmaCompass offers a list of Crotamiton 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 Crotamiton manufacturer or Crotamiton supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Crotamiton manufacturer or Crotamiton supplier.
PharmaCompass also assists you with knowing the Crotamiton API Price utilized in the formulation of products. Crotamiton API Price is not always fixed or binding as the Crotamiton Price is obtained through a variety of data sources. The Crotamiton Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Eurax manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Eurax, including repackagers and relabelers. The FDA regulates Eurax manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Eurax 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 Eurax manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Eurax supplier is an individual or a company that provides Eurax active pharmaceutical ingredient (API) or Eurax finished formulations upon request. The Eurax suppliers may include Eurax API manufacturers, exporters, distributors and traders.
click here to find a list of Eurax 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 Eurax Drug Master File in Japan (Eurax JDMF) empowers Eurax 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 Eurax JDMF during the approval evaluation for pharmaceutical products. At the time of Eurax 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 Eurax suppliers with JDMF on PharmaCompass.
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