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01 Jiangsu Hi-Stone Pharmaceutical Co. , Ltd. (1)
02 Quimica Syntetica S. A. (1)
01 Ranitidine hydrochloride (2)
01 China (1)
02 Spain (1)
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PharmaCompass offers a list of Ranitidine 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 Ranitidine Hydrochloride manufacturer or Ranitidine Hydrochloride supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Ranitidine Hydrochloride manufacturer or Ranitidine Hydrochloride supplier.
PharmaCompass also assists you with knowing the Ranitidine Hydrochloride API Price utilized in the formulation of products. Ranitidine Hydrochloride API Price is not always fixed or binding as the Ranitidine Hydrochloride Price is obtained through a variety of data sources. The Ranitidine Hydrochloride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Alquen manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Alquen, including repackagers and relabelers. The FDA regulates Alquen manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Alquen 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 Alquen manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Alquen supplier is an individual or a company that provides Alquen active pharmaceutical ingredient (API) or Alquen finished formulations upon request. The Alquen suppliers may include Alquen API manufacturers, exporters, distributors and traders.
click here to find a list of Alquen 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 Alquen Drug Master File in Japan (Alquen JDMF) empowers Alquen 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 Alquen JDMF during the approval evaluation for pharmaceutical products. At the time of Alquen 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 Alquen suppliers with JDMF on PharmaCompass.
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