Registration Number : 218MF10770
Registrant's Address : Strada Rivoltana Km 6/7 20090 Rodano Milano Italy
Initial Date of Registration : 2006-09-22
Latest Date of Registration : 2006-09-22
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PharmaCompass offers a list of Bumetanide 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 Bumetanide manufacturer or Bumetanide supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Bumetanide manufacturer or Bumetanide supplier.
PharmaCompass also assists you with knowing the Bumetanide API Price utilized in the formulation of products. Bumetanide API Price is not always fixed or binding as the Bumetanide Price is obtained through a variety of data sources. The Bumetanide Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A BUMETAMIDE USP manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of BUMETAMIDE USP, including repackagers and relabelers. The FDA regulates BUMETAMIDE USP manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. BUMETAMIDE USP 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 BUMETAMIDE USP manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A BUMETAMIDE USP supplier is an individual or a company that provides BUMETAMIDE USP active pharmaceutical ingredient (API) or BUMETAMIDE USP finished formulations upon request. The BUMETAMIDE USP suppliers may include BUMETAMIDE USP API manufacturers, exporters, distributors and traders.
click here to find a list of BUMETAMIDE USP 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 BUMETAMIDE USP Drug Master File in Japan (BUMETAMIDE USP JDMF) empowers BUMETAMIDE USP 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 BUMETAMIDE USP JDMF during the approval evaluation for pharmaceutical products. At the time of BUMETAMIDE USP JDMF registration, PMDA checks if the format is accurate, if the necessary items have been included (application), and if data has been attached.
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