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