01 1Chongqing Huapont Shengchem Pharm. Co. , Ltd.
01 1Diaphenylsulfone (Dapsone)
01 1China
Registration Number : 307MF10152
Registrant's Address : No. 69 Xingguang Avenue, Renhe Town, Yubei District, Chongqing, China
Initial Date of Registration : 2025-12-17
Latest Date of Registration : 2025-12-17
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PharmaCompass offers a list of Dapsone 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 Dapsone manufacturer or Dapsone supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Dapsone manufacturer or Dapsone supplier.
PharmaCompass also assists you with knowing the Dapsone API Price utilized in the formulation of products. Dapsone API Price is not always fixed or binding as the Dapsone Price is obtained through a variety of data sources. The Dapsone Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Novophone manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Novophone, including repackagers and relabelers. The FDA regulates Novophone manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Novophone 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 Novophone manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Novophone supplier is an individual or a company that provides Novophone active pharmaceutical ingredient (API) or Novophone finished formulations upon request. The Novophone suppliers may include Novophone API manufacturers, exporters, distributors and traders.
click here to find a list of Novophone 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 Novophone Drug Master File in Japan (Novophone JDMF) empowers Novophone 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 Novophone JDMF during the approval evaluation for pharmaceutical products. At the time of Novophone 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 Novophone suppliers with JDMF on PharmaCompass.
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