01 1Dipharma Francis S. r. l.
02 1Osaka Synthetic Organic Chemistry Laboratory Co., Ltd.
03 1Procos S. p. A.
01 1Minodronic Acid monohydrate
02 1Minodronic acid hydrate
03 1Minodronic acid hydrate production-only
01 2Italy
02 1Japan
Registration Number : 228MF10082
Registrant's Address : Via Bissone, 5, 20021-Baranzate, Milano, Italy
Initial Date of Registration : 2016-04-06
Latest Date of Registration : 2016-04-06
Minodronic acid hydrate For manufacturing purposes only
Registration Number : 229MF10049
Registrant's Address : 1-1-2 Nishinomiyahama, Nishinomiya City, Hyogo Prefecture
Initial Date of Registration : 2017-02-22
Latest Date of Registration : 2018-05-01
Registration Number : 229MF10035
Registrant's Address : Via Matteotti 249,28062 CAMERI (NOVARA)/ITALY
Initial Date of Registration : 2017-02-08
Latest Date of Registration : 2017-02-08
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PharmaCompass offers a list of Minodronic Acid 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 Minodronic Acid manufacturer or Minodronic Acid supplier for your needs.
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PharmaCompass also assists you with knowing the Minodronic Acid API Price utilized in the formulation of products. Minodronic Acid API Price is not always fixed or binding as the Minodronic Acid Price is obtained through a variety of data sources. The Minodronic Acid Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Bonoteo (TN) manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Bonoteo (TN), including repackagers and relabelers. The FDA regulates Bonoteo (TN) manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Bonoteo (TN) 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 Bonoteo (TN) supplier is an individual or a company that provides Bonoteo (TN) active pharmaceutical ingredient (API) or Bonoteo (TN) finished formulations upon request. The Bonoteo (TN) suppliers may include Bonoteo (TN) API manufacturers, exporters, distributors and traders.
click here to find a list of Bonoteo (TN) 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 Bonoteo (TN) Drug Master File in Japan (Bonoteo (TN) JDMF) empowers Bonoteo (TN) 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 Bonoteo (TN) JDMF during the approval evaluation for pharmaceutical products. At the time of Bonoteo (TN) 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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