01 1D. K. Pharma Chem Pvt. Ltd.
01 1Probenecid
01 1India
Registration Number : 222MF10032
Registrant's Address : W-7, MIDC, Badlapur, Maharashtra, India
Initial Date of Registration : 2010-01-26
Latest Date of Registration : 2010-01-26
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PharmaCompass offers a list of Probenecid 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 Probenecid manufacturer or Probenecid supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Probenecid manufacturer or Probenecid supplier.
PharmaCompass also assists you with knowing the Probenecid API Price utilized in the formulation of products. Probenecid API Price is not always fixed or binding as the Probenecid Price is obtained through a variety of data sources. The Probenecid Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Urocid manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Urocid, including repackagers and relabelers. The FDA regulates Urocid manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Urocid 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 Urocid manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Urocid supplier is an individual or a company that provides Urocid active pharmaceutical ingredient (API) or Urocid finished formulations upon request. The Urocid suppliers may include Urocid API manufacturers, exporters, distributors and traders.
click here to find a list of Urocid 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 Urocid Drug Master File in Japan (Urocid JDMF) empowers Urocid 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 Urocid JDMF during the approval evaluation for pharmaceutical products. At the time of Urocid 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 Urocid suppliers with JDMF on PharmaCompass.
