01 1Alps Pharmaceutical Co., Ltd.
01 1Methylsulfate N- methyl scopolamine
01 1Japan
N-Methylscopolamine methylsulfate
Registration Number : 217MF11029
Registrant's Address : 2-10-50 Mukaimachi, Furukawa-cho, Hida-shi, Gifu Prefecture
Initial Date of Registration : 2005-12-02
Latest Date of Registration : 2009-10-19
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PharmaCompass offers a list of Methscopolamine 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 Methscopolamine Bromide manufacturer or Methscopolamine Bromide supplier for your needs.
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PharmaCompass also assists you with knowing the Methscopolamine Bromide API Price utilized in the formulation of products. Methscopolamine Bromide API Price is not always fixed or binding as the Methscopolamine Bromide Price is obtained through a variety of data sources. The Methscopolamine Bromide Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Hyoscine Methobromide manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Hyoscine Methobromide, including repackagers and relabelers. The FDA regulates Hyoscine Methobromide manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Hyoscine Methobromide API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
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A Hyoscine Methobromide supplier is an individual or a company that provides Hyoscine Methobromide active pharmaceutical ingredient (API) or Hyoscine Methobromide finished formulations upon request. The Hyoscine Methobromide suppliers may include Hyoscine Methobromide API manufacturers, exporters, distributors and traders.
click here to find a list of Hyoscine Methobromide 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 Hyoscine Methobromide Drug Master File in Japan (Hyoscine Methobromide JDMF) empowers Hyoscine Methobromide 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 Hyoscine Methobromide JDMF during the approval evaluation for pharmaceutical products. At the time of Hyoscine Methobromide 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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