PMC Isochem is your partner for smart CDMOs of Intermediates, APIs, & excipients & a catalog of Intermediates & Generic APIs.
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01 1PMC ISOCHEM
02 1Cambrex Profarmaco Milano S. r. l.
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01 1Amiodarone Hydrochloride
02 1Hydrochloric acid amiodarone
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01 1France
02 1U.S.A
PMC Isochem is your partner for smart CDMOs of Intermediates, APIs, & excipients & a catalog of Intermediates & Generic APIs.
Registration Number : 226MF10094
Registrant's Address : 32 Rue Lavoisier 91710 Vert-Le-Petit, France
Initial Date of Registration : 2014-05-14
Latest Date of Registration : 2022-03-02
Registration Number : 218MF10853
Registrant's Address : Via Curiel 34, 20067 Paulo, Milano, ITALY
Initial Date of Registration : 2006-10-20
Latest Date of Registration : 2021-04-08
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PharmaCompass offers a list of Amiodarone Hydrochloride 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 Hydrochloride manufacturer or Amiodarone Hydrochloride supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Amiodarone Hydrochloride manufacturer or Amiodarone Hydrochloride supplier.
PharmaCompass also assists you with knowing the Amiodarone Hydrochloride API Price utilized in the formulation of products. Amiodarone Hydrochloride API Price is not always fixed or binding as the Amiodarone Hydrochloride Price is obtained through a variety of data sources. The Amiodarone Hydrochloride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Aratac manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Aratac, including repackagers and relabelers. The FDA regulates Aratac manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Aratac 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 Aratac manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Aratac supplier is an individual or a company that provides Aratac active pharmaceutical ingredient (API) or Aratac finished formulations upon request. The Aratac suppliers may include Aratac API manufacturers, exporters, distributors and traders.
click here to find a list of Aratac 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 Aratac Drug Master File in Japan (Aratac JDMF) empowers Aratac 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 Aratac JDMF during the approval evaluation for pharmaceutical products. At the time of Aratac 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 Aratac suppliers with JDMF on PharmaCompass.
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