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
A Methscopolamine Bromide manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Methscopolamine Bromide, including repackagers and relabelers. The FDA regulates Methscopolamine Bromide manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Methscopolamine Bromide 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 Methscopolamine Bromide manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Methscopolamine Bromide supplier is an individual or a company that provides Methscopolamine Bromide active pharmaceutical ingredient (API) or Methscopolamine Bromide finished formulations upon request. The Methscopolamine Bromide suppliers may include Methscopolamine Bromide API manufacturers, exporters, distributors and traders.
click here to find a list of Methscopolamine Bromide 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 Methscopolamine Bromide Drug Master File in Japan (Methscopolamine Bromide JDMF) empowers Methscopolamine Bromide 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 Methscopolamine Bromide JDMF during the approval evaluation for pharmaceutical products. At the time of Methscopolamine Bromide 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 Methscopolamine Bromide suppliers with JDMF on PharmaCompass.
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