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01 ESTECHPHARMA CO., LTD. (1)
02 Ouchi Shinko Chemical Industry Co., Ltd. (1)
01 Bunazosin hydrochloride (1)
02 Japanese Pharmacopoeia bunazosin hydrochloride (production only) (1)
01 Japan (1)
02 South Korea (1)
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PharmaCompass offers a list of Bunazosin 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 Bunazosin Hydrochloride manufacturer or Bunazosin Hydrochloride supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Bunazosin Hydrochloride manufacturer or Bunazosin Hydrochloride supplier.
PharmaCompass also assists you with knowing the Bunazosin Hydrochloride API Price utilized in the formulation of products. Bunazosin Hydrochloride API Price is not always fixed or binding as the Bunazosin Hydrochloride Price is obtained through a variety of data sources. The Bunazosin Hydrochloride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A bunazosin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of bunazosin, including repackagers and relabelers. The FDA regulates bunazosin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. bunazosin 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 bunazosin supplier is an individual or a company that provides bunazosin active pharmaceutical ingredient (API) or bunazosin finished formulations upon request. The bunazosin suppliers may include bunazosin API manufacturers, exporters, distributors and traders.
click here to find a list of bunazosin 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 bunazosin Drug Master File in Japan (bunazosin JDMF) empowers bunazosin 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 bunazosin JDMF during the approval evaluation for pharmaceutical products. At the time of bunazosin 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 bunazosin suppliers with JDMF on PharmaCompass.
We have 2 companies offering bunazosin
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