01 1Wuhan Wuyao Pharmaceutical Co. , Ltd.
02 1Yatsushiro Pharmaceutical Co., Ltd.
01 2Sulpyrine hydrate
01 1China
02 1Blank
Registration Number : 229MF10033
Registrant's Address : Room No. 1-6, Floor 23, Building 1#, No. 160 Qiaokou Road Qiaokou District
Initial Date of Registration : 2017-02-08
Latest Date of Registration : 2017-02-08
Registration Number : 222MF10084
Registrant's Address : 10-2 Yoshida Shimojima, Higashiosaka City, Osaka Prefecture
Initial Date of Registration : 2010-03-16
Latest Date of Registration : 2010-03-16
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PharmaCompass offers a list of Metamizole 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 Metamizole manufacturer or Metamizole supplier for your needs.
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PharmaCompass also assists you with knowing the Metamizole API Price utilized in the formulation of products. Metamizole API Price is not always fixed or binding as the Metamizole Price is obtained through a variety of data sources. The Metamizole Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Metamizole Sodium manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Metamizole Sodium, including repackagers and relabelers. The FDA regulates Metamizole Sodium manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Metamizole Sodium 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 Metamizole Sodium supplier is an individual or a company that provides Metamizole Sodium active pharmaceutical ingredient (API) or Metamizole Sodium finished formulations upon request. The Metamizole Sodium suppliers may include Metamizole Sodium API manufacturers, exporters, distributors and traders.
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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 Metamizole Sodium Drug Master File in Japan (Metamizole Sodium JDMF) empowers Metamizole Sodium 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 Metamizole Sodium JDMF during the approval evaluation for pharmaceutical products. At the time of Metamizole Sodium 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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