01 1Sumitomo Chemical Co., Ltd.
01 1Japanese Pharmacopoeia trientine hydrochloride
01 1Japan
Japanese Pharmacopoeia Trientine Hydrochloride
Registration Number : 218MF10740
Registrant's Address : 2-27-1 Shinkawa, Chuo-ku, Tokyo
Initial Date of Registration : 2006-09-06
Latest Date of Registration : 2006-09-06
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PharmaCompass offers a list of Trientine Hydrochloride 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 Trientine Hydrochloride manufacturer or Trientine Hydrochloride supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Trientine Hydrochloride manufacturer or Trientine Hydrochloride supplier.
PharmaCompass also assists you with knowing the Trientine Hydrochloride API Price utilized in the formulation of products. Trientine Hydrochloride API Price is not always fixed or binding as the Trientine Hydrochloride Price is obtained through a variety of data sources. The Trientine Hydrochloride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A 38260-01-4 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of 38260-01-4, including repackagers and relabelers. The FDA regulates 38260-01-4 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. 38260-01-4 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 38260-01-4 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A 38260-01-4 supplier is an individual or a company that provides 38260-01-4 active pharmaceutical ingredient (API) or 38260-01-4 finished formulations upon request. The 38260-01-4 suppliers may include 38260-01-4 API manufacturers, exporters, distributors and traders.
click here to find a list of 38260-01-4 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 38260-01-4 Drug Master File in Japan (38260-01-4 JDMF) empowers 38260-01-4 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 38260-01-4 JDMF during the approval evaluation for pharmaceutical products. At the time of 38260-01-4 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 38260-01-4 suppliers with JDMF on PharmaCompass.
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