01 1Alps Pharmaceutical Co., Ltd.
01 1Japanese Pharmacopoeia Butoropiumu bromide
01 1Japan
Japanese Pharmacopoeia Butropium Bromide
Registration Number : 221MF10173
Registrant's Address : 2-10-50 Mukaimachi, Furukawa-cho, Hida-shi, Gifu Prefecture
Initial Date of Registration : 2009-07-30
Latest Date of Registration : 2009-07-30
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PharmaCompass offers a list of Tiotropium Bromide 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 Tiotropium Bromide manufacturer or Tiotropium Bromide supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Tiotropium Bromide manufacturer or Tiotropium Bromide supplier.
PharmaCompass also assists you with knowing the Tiotropium Bromide API Price utilized in the formulation of products. Tiotropium Bromide API Price is not always fixed or binding as the Tiotropium Bromide Price is obtained through a variety of data sources. The Tiotropium Bromide Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Respimat manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Respimat, including repackagers and relabelers. The FDA regulates Respimat manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Respimat 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 Respimat manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Respimat supplier is an individual or a company that provides Respimat active pharmaceutical ingredient (API) or Respimat finished formulations upon request. The Respimat suppliers may include Respimat API manufacturers, exporters, distributors and traders.
click here to find a list of Respimat 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 Respimat Drug Master File in Japan (Respimat JDMF) empowers Respimat 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 Respimat JDMF during the approval evaluation for pharmaceutical products. At the time of Respimat 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 Respimat suppliers with JDMF on PharmaCompass.
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