01 1Hamari PFST Co., Ltd.
02 1Yamamoto Chemical Industry Co., Ltd.
01 1Buformin hydrochloride "hamari Y"
02 1Japanese Pharmacopoeia buformin hydrochloride
01 2Japan
Japanese Pharmacopoeia Buformin Hydrochloride
Registration Number : 220MF10168
Registrant's Address : 1-4 Funatsucho, Wakayama City, Wakayama Prefecture
Initial Date of Registration : 2008-07-24
Latest Date of Registration : 2008-07-24
Buformin hydrochloride "Hamari Y"
Registration Number : 222MF10139
Registrant's Address : Osaka Prefecture, Osaka City, Suminoe Ward, Nanko Kita 1-19-40
Initial Date of Registration : 2010-04-14
Latest Date of Registration : 2010-04-14
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PharmaCompass offers a list of 1190-53-0 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 1190-53-0 manufacturer or 1190-53-0 supplier for your needs.
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PharmaCompass also assists you with knowing the 1190-53-0 API Price utilized in the formulation of products. 1190-53-0 API Price is not always fixed or binding as the 1190-53-0 Price is obtained through a variety of data sources. The 1190-53-0 Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Diabrin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Diabrin, including repackagers and relabelers. The FDA regulates Diabrin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Diabrin API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
A Diabrin supplier is an individual or a company that provides Diabrin active pharmaceutical ingredient (API) or Diabrin finished formulations upon request. The Diabrin suppliers may include Diabrin API manufacturers, exporters, distributors and traders.
click here to find a list of Diabrin 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 Diabrin Drug Master File in Japan (Diabrin JDMF) empowers Diabrin 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 Diabrin JDMF during the approval evaluation for pharmaceutical products. At the time of Diabrin 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 Diabrin suppliers with JDMF on PharmaCompass.
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