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 ALBB-025846 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of ALBB-025846, including repackagers and relabelers. The FDA regulates ALBB-025846 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. ALBB-025846 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 ALBB-025846 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A ALBB-025846 supplier is an individual or a company that provides ALBB-025846 active pharmaceutical ingredient (API) or ALBB-025846 finished formulations upon request. The ALBB-025846 suppliers may include ALBB-025846 API manufacturers, exporters, distributors and traders.
click here to find a list of ALBB-025846 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 ALBB-025846 Drug Master File in Japan (ALBB-025846 JDMF) empowers ALBB-025846 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 ALBB-025846 JDMF during the approval evaluation for pharmaceutical products. At the time of ALBB-025846 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 ALBB-025846 suppliers with JDMF on PharmaCompass.
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