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
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
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
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
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
57
PharmaCompass offers a list of Magnesium Oxide 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 Oxide manufacturer or Magnesium Oxide supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Magnesium Oxide manufacturer or Magnesium Oxide supplier.
PharmaCompass also assists you with knowing the Magnesium Oxide API Price utilized in the formulation of products. Magnesium Oxide API Price is not always fixed or binding as the Magnesium Oxide Price is obtained through a variety of data sources. The Magnesium Oxide Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Luvatol MK 35 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Luvatol MK 35, including repackagers and relabelers. The FDA regulates Luvatol MK 35 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Luvatol MK 35 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 Luvatol MK 35 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Luvatol MK 35 supplier is an individual or a company that provides Luvatol MK 35 active pharmaceutical ingredient (API) or Luvatol MK 35 finished formulations upon request. The Luvatol MK 35 suppliers may include Luvatol MK 35 API manufacturers, exporters, distributors and traders.
click here to find a list of Luvatol MK 35 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 Luvatol MK 35 Drug Master File in Japan (Luvatol MK 35 JDMF) empowers Luvatol MK 35 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 Luvatol MK 35 JDMF during the approval evaluation for pharmaceutical products. At the time of Luvatol MK 35 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 Luvatol MK 35 suppliers with JDMF on PharmaCompass.
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