01 2Tokyo Chemical Industry Co., Ltd.
01 1Methyl sulfate neostigmine
02 1Neostigmine bromide
01 2Japan
Registration Number : 217MF11160
Registrant's Address : 6-15-9 Toshima, Kita-ku, Tokyo
Initial Date of Registration : 2005-12-12
Latest Date of Registration : 2006-10-20
Registration Number : 217MF11158
Registrant's Address : 6-15-9 Toshima, Kita-ku, Tokyo
Initial Date of Registration : 2005-12-12
Latest Date of Registration : 2006-10-20
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PharmaCompass offers a list of Neostigmine Methyl Sulfate 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 Neostigmine Methyl Sulfate manufacturer or Neostigmine Methyl Sulfate supplier for your needs.
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PharmaCompass also assists you with knowing the Neostigmine Methyl Sulfate API Price utilized in the formulation of products. Neostigmine Methyl Sulfate API Price is not always fixed or binding as the Neostigmine Methyl Sulfate Price is obtained through a variety of data sources. The Neostigmine Methyl Sulfate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Neostigmine Methylsulfate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Neostigmine Methylsulfate, including repackagers and relabelers. The FDA regulates Neostigmine Methylsulfate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Neostigmine 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.
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A Neostigmine Methylsulfate supplier is an individual or a company that provides Neostigmine Methylsulfate active pharmaceutical ingredient (API) or Neostigmine Methylsulfate finished formulations upon request. The Neostigmine Methylsulfate suppliers may include Neostigmine Methylsulfate API manufacturers, exporters, distributors and traders.
click here to find a list of Neostigmine 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 Neostigmine Methylsulfate Drug Master File in Japan (Neostigmine Methylsulfate JDMF) empowers Neostigmine 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 Neostigmine Methylsulfate JDMF during the approval evaluation for pharmaceutical products. At the time of Neostigmine Methylsulfate 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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