01 1Jiangsu Hi-Stone Pharmaceutical Co. , Ltd.
02 1Quimica Syntetica S. A.
01 2Ranitidine hydrochloride
01 1China
02 1Spain
Registration Number : 218MF10877
Registrant's Address : Yaozhen Village, Zhitang Town, Changshu City, Jiangsu Province, China
Initial Date of Registration : 2006-11-10
Latest Date of Registration : 2006-11-10
Registration Number : 226MF10189
Registrant's Address : Calle Dulcinea, s/n 28805 Alcala De Henares Madrid Spain
Initial Date of Registration : 2014-09-30
Latest Date of Registration : 2014-09-30
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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 Zantac 25 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Zantac 25, including repackagers and relabelers. The FDA regulates Zantac 25 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Zantac 25 API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
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A Zantac 25 supplier is an individual or a company that provides Zantac 25 active pharmaceutical ingredient (API) or Zantac 25 finished formulations upon request. The Zantac 25 suppliers may include Zantac 25 API manufacturers, exporters, distributors and traders.
click here to find a list of Zantac 25 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 Zantac 25 Drug Master File in Japan (Zantac 25 JDMF) empowers Zantac 25 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 Zantac 25 JDMF during the approval evaluation for pharmaceutical products. At the time of Zantac 25 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 Zantac 25 suppliers with JDMF on PharmaCompass.
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