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
DUOLITET.M. 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
A Cholestyramine manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Cholestyramine, including repackagers and relabelers. The FDA regulates Cholestyramine manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Cholestyramine 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 Cholestyramine manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Cholestyramine supplier is an individual or a company that provides Cholestyramine active pharmaceutical ingredient (API) or Cholestyramine finished formulations upon request. The Cholestyramine suppliers may include Cholestyramine API manufacturers, exporters, distributors and traders.
click here to find a list of Cholestyramine 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 Cholestyramine Drug Master File in Japan (Cholestyramine JDMF) empowers Cholestyramine 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 Cholestyramine JDMF during the approval evaluation for pharmaceutical products. At the time of Cholestyramine 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 Cholestyramine suppliers with JDMF on PharmaCompass.
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