01 1DSP
02 1S. C. PUROLITE S. R. L.
01 1Cholestyramine
02 1DUOLITETM AP143 / 1083, Cholestyramine
01 1U.S.A
02 1United Kingdom
Registration Number : 223MF10027
Registrant's Address : Str. Aleeea Uzinei Nr. 11, 505700 Victoria, Judetul Brasov, Romania
Initial Date of Registration : 2011-02-25
Latest Date of Registration : 2011-02-25
DUOLITETM AP143/1083, Cholestyramine
Registration Number : 228MF10132
Registrant's Address : 22 Rue Brunel 75017 Paris France
Initial Date of Registration : 2016-07-25
Latest Date of Registration : 2023-03-07
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PharmaCompass offers a list of Cholestyramine 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 Cholestyramine manufacturer or Cholestyramine supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Cholestyramine manufacturer or Cholestyramine supplier.
PharmaCompass also assists you with knowing the Cholestyramine API Price utilized in the formulation of products. Cholestyramine API Price is not always fixed or binding as the Cholestyramine Price is obtained through a variety of data sources. The Cholestyramine Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A QUESTRAN LIGHT manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of QUESTRAN LIGHT, including repackagers and relabelers. The FDA regulates QUESTRAN LIGHT manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. QUESTRAN LIGHT 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 QUESTRAN LIGHT manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A QUESTRAN LIGHT supplier is an individual or a company that provides QUESTRAN LIGHT active pharmaceutical ingredient (API) or QUESTRAN LIGHT finished formulations upon request. The QUESTRAN LIGHT suppliers may include QUESTRAN LIGHT API manufacturers, exporters, distributors and traders.
click here to find a list of QUESTRAN LIGHT 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 QUESTRAN LIGHT Drug Master File in Japan (QUESTRAN LIGHT JDMF) empowers QUESTRAN LIGHT 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 QUESTRAN LIGHT JDMF during the approval evaluation for pharmaceutical products. At the time of QUESTRAN LIGHT 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 QUESTRAN LIGHT suppliers with JDMF on PharmaCompass.
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