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.
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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 DivK1c_000508 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of DivK1c_000508, including repackagers and relabelers. The FDA regulates DivK1c_000508 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. DivK1c_000508 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 DivK1c_000508 supplier is an individual or a company that provides DivK1c_000508 active pharmaceutical ingredient (API) or DivK1c_000508 finished formulations upon request. The DivK1c_000508 suppliers may include DivK1c_000508 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 DivK1c_000508 Drug Master File in Japan (DivK1c_000508 JDMF) empowers DivK1c_000508 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 DivK1c_000508 JDMF during the approval evaluation for pharmaceutical products. At the time of DivK1c_000508 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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