01 1DIFC CO. ,LTD
02 1ERCROS S. A.
03 1Ipca Laboratories Limited
04 2Ohara Pharmaceutical Co., Ltd.
05 1Phalanx Labs Private Limited
06 2Quimica Syntetica S. A.
07 2SMS Pharmaceuticals Limited
08 1UK Chemipharm Co. , Ltd.
09 2Yoshindo Co., Ltd.
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PharmaCompass offers a list of Famotidine 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 Famotidine manufacturer or Famotidine supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Famotidine manufacturer or Famotidine supplier.
PharmaCompass also assists you with knowing the Famotidine API Price utilized in the formulation of products. Famotidine API Price is not always fixed or binding as the Famotidine Price is obtained through a variety of data sources. The Famotidine Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Bio-0739 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Bio-0739, including repackagers and relabelers. The FDA regulates Bio-0739 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Bio-0739 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 Bio-0739 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Bio-0739 supplier is an individual or a company that provides Bio-0739 active pharmaceutical ingredient (API) or Bio-0739 finished formulations upon request. The Bio-0739 suppliers may include Bio-0739 API manufacturers, exporters, distributors and traders.
click here to find a list of Bio-0739 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 Bio-0739 Drug Master File in Japan (Bio-0739 JDMF) empowers Bio-0739 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 Bio-0739 JDMF during the approval evaluation for pharmaceutical products. At the time of Bio-0739 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 Bio-0739 suppliers with JDMF on PharmaCompass.
We have 9 companies offering Bio-0739
Get in contact with the supplier of your choice:
