01 1Cambrex Profarmaco Milano S. r. l.
02 1RECORDATI INDUSTRIA CHIMICA E FARMACEUTICA S. P. A.
01 1Cysteamine Tartrate
02 1Cysteamine bitartrate
01 1Italy
02 1U.S.A
Registration Number : 225MF10146
Registrant's Address : Via Curiel 34, 20067 Paulo, Milano, ITALY
Initial Date of Registration : 2013-07-25
Latest Date of Registration : 2023-02-15
Registration Number : 305MF10033
Registrant's Address : VIA M. Civitali, 1-20148 MILANO, ITALY
Initial Date of Registration : 2023-03-15
Latest Date of Registration : 2023-03-15
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PharmaCompass offers a list of Cysteamine Bitartrate 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 Cysteamine Bitartrate manufacturer or Cysteamine Bitartrate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Cysteamine Bitartrate manufacturer or Cysteamine Bitartrate supplier.
PharmaCompass also assists you with knowing the Cysteamine Bitartrate API Price utilized in the formulation of products. Cysteamine Bitartrate API Price is not always fixed or binding as the Cysteamine Bitartrate Price is obtained through a variety of data sources. The Cysteamine Bitartrate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Cysteamine Bitartrate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Cysteamine Bitartrate, including repackagers and relabelers. The FDA regulates Cysteamine Bitartrate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Cysteamine Bitartrate 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 Cysteamine Bitartrate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Cysteamine Bitartrate supplier is an individual or a company that provides Cysteamine Bitartrate active pharmaceutical ingredient (API) or Cysteamine Bitartrate finished formulations upon request. The Cysteamine Bitartrate suppliers may include Cysteamine Bitartrate API manufacturers, exporters, distributors and traders.
click here to find a list of Cysteamine Bitartrate 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 Cysteamine Bitartrate Drug Master File in Japan (Cysteamine Bitartrate JDMF) empowers Cysteamine Bitartrate 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 Cysteamine Bitartrate JDMF during the approval evaluation for pharmaceutical products. At the time of Cysteamine Bitartrate 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 Cysteamine Bitartrate suppliers with JDMF on PharmaCompass.
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