01 5Tomita Pharmaceutical Co., Ltd.
01 1Japanese Pharmacopoeia Magnesium Sulfate Hydrate
02 1Japanese Pharmacopoeia magnesium sulfate hydrate
03 1Japanese Pharmacopoeia magnesium sulfate hydrate 60M
04 1Magnesium sulfate, "Tomita"
05 1Magnesium sulfate, "Tomita" 60M
01 5Japan
Japanese Pharmacopoeia Magnesium Sulfate Hydrate
Registration Number : 306MF10162
Registrant's Address : Tokushima Prefecture Naruto City Setocho Myojin Maruyama 85-1
Initial Date of Registration : 2024-12-18
Latest Date of Registration : 2024-12-18
Magnesium sulfate "Tomita" 60M
Registration Number : 227MF10134
Registrant's Address : Tokushima Prefecture Naruto City Setocho Myojin Maruyama 85-1
Initial Date of Registration : 2015-04-30
Latest Date of Registration : 2015-04-30
Japanese Pharmacopoeia Magnesium Sulfate Hydrate 60M
Registration Number : 228MF10106
Registrant's Address : Tokushima Prefecture Naruto City Setocho Myojin Maruyama 85-1
Initial Date of Registration : 2016-06-06
Latest Date of Registration : 2016-06-06
Japanese Pharmacopoeia Magnesium Sulfate Hydrate
Registration Number : 227MF10096
Registrant's Address : Tokushima Prefecture Naruto City Setocho Myojin Maruyama 85-1
Initial Date of Registration : 2015-03-20
Latest Date of Registration : 2015-03-20
Registration Number : 217MF10525
Registrant's Address : Tokushima Prefecture Naruto City Setocho Myojin Maruyama 85-1
Initial Date of Registration : 2005-09-07
Latest Date of Registration : 2006-07-20
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PharmaCompass offers a list of Magnesium 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 Magnesium Sulfate manufacturer or Magnesium Sulfate supplier for your needs.
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PharmaCompass also assists you with knowing the Magnesium Sulfate API Price utilized in the formulation of products. Magnesium Sulfate API Price is not always fixed or binding as the Magnesium Sulfate Price is obtained through a variety of data sources. The Magnesium Sulfate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A SUPREP BOWEL PREP KIT manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of SUPREP BOWEL PREP KIT, including repackagers and relabelers. The FDA regulates SUPREP BOWEL PREP KIT manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. SUPREP BOWEL PREP KIT 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 SUPREP BOWEL PREP KIT supplier is an individual or a company that provides SUPREP BOWEL PREP KIT active pharmaceutical ingredient (API) or SUPREP BOWEL PREP KIT finished formulations upon request. The SUPREP BOWEL PREP KIT suppliers may include SUPREP BOWEL PREP KIT API manufacturers, exporters, distributors and traders.
click here to find a list of SUPREP BOWEL PREP KIT 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 SUPREP BOWEL PREP KIT Drug Master File in Japan (SUPREP BOWEL PREP KIT JDMF) empowers SUPREP BOWEL PREP KIT 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 SUPREP BOWEL PREP KIT JDMF during the approval evaluation for pharmaceutical products. At the time of SUPREP BOWEL PREP KIT 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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