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