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
A Minodronic Acid manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Minodronic Acid, including repackagers and relabelers. The FDA regulates Minodronic Acid manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Minodronic Acid 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 Minodronic Acid manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Minodronic Acid supplier is an individual or a company that provides Minodronic Acid active pharmaceutical ingredient (API) or Minodronic Acid finished formulations upon request. The Minodronic Acid suppliers may include Minodronic Acid API manufacturers, exporters, distributors and traders.
click here to find a list of Minodronic Acid 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 Minodronic Acid Drug Master File in Japan (Minodronic Acid JDMF) empowers Minodronic Acid 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 Minodronic Acid JDMF during the approval evaluation for pharmaceutical products. At the time of Minodronic Acid 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 Minodronic Acid suppliers with JDMF on PharmaCompass.
We have 3 companies offering Minodronic Acid
Get in contact with the supplier of your choice:
LOOKING FOR A SUPPLIER?
