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