01 12Kyowa Chemical Industry Co., Ltd.
02 3Tomita Pharmaceutical Co., Ltd.
01 1Heavy Magnesium Oxide JP
02 1Heavy magnesium oxide "Tomita"
03 2Japanese Pharmacopoeia Magnesium Oxide (for manufacturing only)
04 1Japanese Pharmacopoeia heavy magnesium oxide (fine) PL
05 9Japanese Pharmacopoeia magnesium oxide (production only)
06 1Magnesium Oxide, USP
01 15Japan
Japanese Pharmacopoeia Magnesium Oxide (for manufacturing only)
Registration Number : 301MF10079
Registrant's Address : 305 Yashima Nishimachi, Takamatsu City, Kagawa Prefecture
Initial Date of Registration : 2019-10-18
Latest Date of Registration : 2019-10-18
Japanese Pharmacopoeia Magnesium Oxide (for manufacturing only)
Registration Number : 301MF10078
Registrant's Address : 305 Yashima Nishimachi, Takamatsu City, Kagawa Prefecture
Initial Date of Registration : 2019-10-18
Latest Date of Registration : 2019-10-18
Registration Number : 222MF10009
Registrant's Address : 305 Yashima Nishimachi, Takamatsu City, Kagawa Prefecture
Initial Date of Registration : 2010-01-07
Latest Date of Registration : 2010-01-07
Japanese Pharmacopoeia Magnesium Oxide (for manufacturing only)
Registration Number : 222MF10008
Registrant's Address : 305 Yashima Nishimachi, Takamatsu City, Kagawa Prefecture
Initial Date of Registration : 2010-01-07
Latest Date of Registration : 2010-01-07
Japanese Pharmacopoeia Magnesium Oxide (for manufacturing only)
Registration Number : 222MF10007
Registrant's Address : 305 Yashima Nishimachi, Takamatsu City, Kagawa Prefecture
Initial Date of Registration : 2010-01-07
Latest Date of Registration : 2010-01-07
Japanese Pharmacopoeia Magnesium Oxide (for manufacturing only)
Registration Number : 222MF10006
Registrant's Address : 305 Yashima Nishimachi, Takamatsu City, Kagawa Prefecture
Initial Date of Registration : 2010-01-07
Latest Date of Registration : 2010-01-07
Japanese Pharmacopoeia Magnesium Oxide (for manufacturing only)
Registration Number : 222MF10005
Registrant's Address : 305 Yashima Nishimachi, Takamatsu City, Kagawa Prefecture
Initial Date of Registration : 2010-01-07
Latest Date of Registration : 2010-01-07
Japanese Pharmacopoeia Magnesium Oxide (for manufacturing only)
Registration Number : 222MF10004
Registrant's Address : 305 Yashima Nishimachi, Takamatsu City, Kagawa Prefecture
Initial Date of Registration : 2010-01-07
Latest Date of Registration : 2010-01-07
Registration Number : 227MF10056
Registrant's Address : Tokushima Prefecture Naruto City Setocho Myojin Maruyama 85-1
Initial Date of Registration : 2015-03-06
Latest Date of Registration : 2015-03-06
Japanese Pharmacopoeia Heavy Magnesium Oxide (Fine Granules) PL
Registration Number : 228MF10224
Registrant's Address : Tokushima Prefecture Naruto City Setocho Myojin Maruyama 85-1
Initial Date of Registration : 2016-11-29
Latest Date of Registration : 2016-11-29
A Magnesium Oxide manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Magnesium Oxide, including repackagers and relabelers. The FDA regulates Magnesium Oxide manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Magnesium Oxide 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 Magnesium Oxide manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Magnesium Oxide supplier is an individual or a company that provides Magnesium Oxide active pharmaceutical ingredient (API) or Magnesium Oxide finished formulations upon request. The Magnesium Oxide suppliers may include Magnesium Oxide API manufacturers, exporters, distributors and traders.
click here to find a list of Magnesium Oxide 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 Magnesium Oxide Drug Master File in Japan (Magnesium Oxide JDMF) empowers Magnesium Oxide 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 Magnesium Oxide JDMF during the approval evaluation for pharmaceutical products. At the time of Magnesium Oxide 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 Magnesium Oxide suppliers with JDMF on PharmaCompass.
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