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 Standards for Non-Official Drugs: 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
25
PharmaCompass offers a list of Crotamiton API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, 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.
A 483-63-6 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of 483-63-6, including repackagers and relabelers. The FDA regulates 483-63-6 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. 483-63-6 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 483-63-6 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A 483-63-6 supplier is an individual or a company that provides 483-63-6 active pharmaceutical ingredient (API) or 483-63-6 finished formulations upon request. The 483-63-6 suppliers may include 483-63-6 API manufacturers, exporters, distributors and traders.
click here to find a list of 483-63-6 suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA 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 483-63-6 Drug Master File in Japan (483-63-6 JDMF) empowers 483-63-6 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 483-63-6 JDMF during the approval evaluation for pharmaceutical products. At the time of 483-63-6 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 483-63-6 suppliers with JDMF on PharmaCompass.
We have 2 companies offering 483-63-6
Get in contact with the supplier of your choice:
