01 1Synthon s. r. o.
01 1Anagrelide Hydrochloride Monohydrate
01 1Netherlands
Anagrelide Hydrochloride Monohydrate
Registration Number : 307MF10030
Registrant's Address : Brnenska 32/cp. 597 678 01 Blansko Czech Republic
Initial Date of Registration : 2025-02-07
Latest Date of Registration : 2025-02-07
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PharmaCompass offers a list of Anagrelide 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 Anagrelide Hydrochloride manufacturer or Anagrelide Hydrochloride supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Anagrelide Hydrochloride manufacturer or Anagrelide Hydrochloride supplier.
PharmaCompass also assists you with knowing the Anagrelide Hydrochloride API Price utilized in the formulation of products. Anagrelide Hydrochloride API Price is not always fixed or binding as the Anagrelide Hydrochloride Price is obtained through a variety of data sources. The Anagrelide Hydrochloride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Thromboreductin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Thromboreductin, including repackagers and relabelers. The FDA regulates Thromboreductin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Thromboreductin 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 Thromboreductin manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Thromboreductin supplier is an individual or a company that provides Thromboreductin active pharmaceutical ingredient (API) or Thromboreductin finished formulations upon request. The Thromboreductin suppliers may include Thromboreductin API manufacturers, exporters, distributors and traders.
click here to find a list of Thromboreductin 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 Thromboreductin Drug Master File in Japan (Thromboreductin JDMF) empowers Thromboreductin 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 Thromboreductin JDMF during the approval evaluation for pharmaceutical products. At the time of Thromboreductin 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 Thromboreductin suppliers with JDMF on PharmaCompass.
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