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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 Alter-H2 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Alter-H2, including repackagers and relabelers. The FDA regulates Alter-H2 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Alter-H2 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 Alter-H2 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Alter-H2 supplier is an individual or a company that provides Alter-H2 active pharmaceutical ingredient (API) or Alter-H2 finished formulations upon request. The Alter-H2 suppliers may include Alter-H2 API manufacturers, exporters, distributors and traders.
click here to find a list of Alter-H2 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 Alter-H2 Drug Master File in Japan (Alter-H2 JDMF) empowers Alter-H2 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 Alter-H2 JDMF during the approval evaluation for pharmaceutical products. At the time of Alter-H2 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 Alter-H2 suppliers with JDMF on PharmaCompass.
We have 2 companies offering Alter-H2
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