01 1Hangzhou Meiya Pharmaceutical Co. , Ltd.
02 2Kyowa Hakko Bio Co., Ltd.
01 1Adenosine 3 ', 5'-cyclic monophosphate
02 2Outsider regulations adenosine triphosphate disodium (manufactured only)
01 1China
02 2Japan
Adenosine 3',5'-cyclic monophosphate
Registration Number : 225MF10199
Registrant's Address : No. 21, Fuqiang Road, Gongshu District, Hangzhou, Zhejiang, China
Initial Date of Registration : 2013-10-23
Latest Date of Registration : 2013-10-23
Adenosine triphosphate disodium (for manufacturing only)
Registration Number : 217MF10262
Registrant's Address : 1-6-1 Otemachi, Chiyoda-ku, Tokyo
Initial Date of Registration : 2005-06-15
Latest Date of Registration : 2006-02-10
Adenosine triphosphate disodium (for manufacturing only)
Registration Number : 229MF10190
Registrant's Address : 1-6-1 Otemachi, Chiyoda-ku, Tokyo
Initial Date of Registration : 2017-10-30
Latest Date of Registration : 2017-10-30
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PharmaCompass offers a list of Adenosine 5'-Monophosphate 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 Adenosine 5'-Monophosphate manufacturer or Adenosine 5'-Monophosphate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Adenosine 5'-Monophosphate manufacturer or Adenosine 5'-Monophosphate supplier.
PharmaCompass also assists you with knowing the Adenosine 5'-Monophosphate API Price utilized in the formulation of products. Adenosine 5'-Monophosphate API Price is not always fixed or binding as the Adenosine 5'-Monophosphate Price is obtained through a variety of data sources. The Adenosine 5'-Monophosphate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A AMP manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of AMP, including repackagers and relabelers. The FDA regulates AMP manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. AMP 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 AMP manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A AMP supplier is an individual or a company that provides AMP active pharmaceutical ingredient (API) or AMP finished formulations upon request. The AMP suppliers may include AMP API manufacturers, exporters, distributors and traders.
click here to find a list of AMP 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 AMP Drug Master File in Japan (AMP JDMF) empowers AMP 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 AMP JDMF during the approval evaluation for pharmaceutical products. At the time of AMP 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 AMP suppliers with JDMF on PharmaCompass.
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