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PharmaCompass offers a list of Amiodarone 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 Amiodarone manufacturer or Amiodarone supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Amiodarone manufacturer or Amiodarone supplier.
PharmaCompass also assists you with knowing the Amiodarone API Price utilized in the formulation of products. Amiodarone API Price is not always fixed or binding as the Amiodarone Price is obtained through a variety of data sources. The Amiodarone Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Amiodarone Hydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Amiodarone Hydrochloride, including repackagers and relabelers. The FDA regulates Amiodarone Hydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Amiodarone Hydrochloride 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 Amiodarone Hydrochloride manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Amiodarone Hydrochloride supplier is an individual or a company that provides Amiodarone Hydrochloride active pharmaceutical ingredient (API) or Amiodarone Hydrochloride finished formulations upon request. The Amiodarone Hydrochloride suppliers may include Amiodarone Hydrochloride API manufacturers, exporters, distributors and traders.
click here to find a list of Amiodarone Hydrochloride 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 Amiodarone Hydrochloride Drug Master File in Japan (Amiodarone Hydrochloride JDMF) empowers Amiodarone Hydrochloride 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 Amiodarone Hydrochloride JDMF during the approval evaluation for pharmaceutical products. At the time of Amiodarone Hydrochloride 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 Amiodarone Hydrochloride suppliers with JDMF on PharmaCompass.
We have 2 companies offering Amiodarone Hydrochloride
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