Registration Number : 217MF10330
Registrant's Address : 13, rue Auguste Desgene (') tais, 76210 Bolbec, FRANCE
Initial Date of Registration : 2005-08-09
Latest Date of Registration : 2021-02-16
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PharmaCompass offers a list of Indapamide 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 Indapamide manufacturer or Indapamide supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Indapamide manufacturer or Indapamide supplier.
PharmaCompass also assists you with knowing the Indapamide API Price utilized in the formulation of products. Indapamide API Price is not always fixed or binding as the Indapamide Price is obtained through a variety of data sources. The Indapamide Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Lozide manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Lozide, including repackagers and relabelers. The FDA regulates Lozide manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Lozide 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 Lozide manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Lozide supplier is an individual or a company that provides Lozide active pharmaceutical ingredient (API) or Lozide finished formulations upon request. The Lozide suppliers may include Lozide API manufacturers, exporters, distributors and traders.
click here to find a list of Lozide 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 Lozide Drug Master File in Japan (Lozide JDMF) empowers Lozide 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 Lozide JDMF during the approval evaluation for pharmaceutical products. At the time of Lozide 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 Lozide suppliers with JDMF on PharmaCompass.
