Minakem is manufacturing small molecules APIs including corticosteroids
01 1Delmar Chemicals Inc.
02 1Biocon Limited
03 1F. I. S. Fabrica Italiana Sintetici S. p. A.
01 3Fluvastatin sodium
01 1Canada
02 1India
03 1Italy
Minakem is manufacturing small molecules APIs including corticosteroids
Registration Number : 220MF10010
Registrant's Address : 9321 Airlie St. , LaSalle, QC, Canada, H8R 2B2
Initial Date of Registration : 2008-01-09
Latest Date of Registration : 2016-12-26
Registration Number : 225MF10102
Registrant's Address : 20th K. M. Hosur Road, Electronics City-560100, Bangalore, India
Initial Date of Registration : 2013-05-13
Latest Date of Registration : 2015-06-18
Registration Number : 224MF10199
Registrant's Address : Viale Milano 26 36075 Montecchio Maggiore Vicenza, Italy
Initial Date of Registration : 2012-10-01
Latest Date of Registration : 2023-02-21
A Fluvastatin Sodium manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Fluvastatin Sodium, including repackagers and relabelers. The FDA regulates Fluvastatin Sodium manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Fluvastatin 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.
click here to find a list of Fluvastatin Sodium manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Fluvastatin Sodium supplier is an individual or a company that provides Fluvastatin Sodium active pharmaceutical ingredient (API) or Fluvastatin Sodium finished formulations upon request. The Fluvastatin Sodium suppliers may include Fluvastatin Sodium API manufacturers, exporters, distributors and traders.
click here to find a list of Fluvastatin Sodium 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 Fluvastatin Sodium Drug Master File in Japan (Fluvastatin Sodium JDMF) empowers Fluvastatin 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 Fluvastatin Sodium JDMF during the approval evaluation for pharmaceutical products. At the time of Fluvastatin Sodium 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 Fluvastatin Sodium suppliers with JDMF on PharmaCompass.
We have 3 companies offering Fluvastatin Sodium
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