01 1Alps Pharmaceutical Co., Ltd.
01 1Scopolamine hydrobromide hydrate
01 1Japan
Scopolamine hydrobromide hydrate
Registration Number : 303MF10050
Registrant's Address : 2-10-50 Mukaimachi, Furukawacho, Hida City, Gifu Prefecture
Initial Date of Registration : 2021-03-22
Latest Date of Registration : 2021-03-22
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PharmaCompass offers a list of Scopolamine 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 Scopolamine manufacturer or Scopolamine supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Scopolamine manufacturer or Scopolamine supplier.
PharmaCompass also assists you with knowing the Scopolamine API Price utilized in the formulation of products. Scopolamine API Price is not always fixed or binding as the Scopolamine Price is obtained through a variety of data sources. The Scopolamine Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Kwells manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Kwells, including repackagers and relabelers. The FDA regulates Kwells manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Kwells 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 Kwells manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Kwells supplier is an individual or a company that provides Kwells active pharmaceutical ingredient (API) or Kwells finished formulations upon request. The Kwells suppliers may include Kwells API manufacturers, exporters, distributors and traders.
click here to find a list of Kwells 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 Kwells Drug Master File in Japan (Kwells JDMF) empowers Kwells 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 Kwells JDMF during the approval evaluation for pharmaceutical products. At the time of Kwells 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 Kwells suppliers with JDMF on PharmaCompass.
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