01 1M/s Sionc Pharmaceuticals Pvt ltd
01 1Sodium Phosphate Dibasic Hepta Hydrate IH/USP
01 1WC-0589
01 1India
Sodium Phosphate Dibasic Hepta Hydrate IH/USP
Date of Issue : 2024-02-08
Valid Till : 2027-01-08
Written Confirmation Number : WC-0589
Address of the Firm : Unit-ll, Plot No. 25 & 25A, J N Pharma City, Parawada (M), Anakapalli -District ...
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PharmaCompass offers a list of Disodium Hydrogen Phosphate 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 Disodium Hydrogen Phosphate manufacturer or Disodium Hydrogen Phosphate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Disodium Hydrogen Phosphate manufacturer or Disodium Hydrogen Phosphate supplier.
PharmaCompass also assists you with knowing the Disodium Hydrogen Phosphate API Price utilized in the formulation of products. Disodium Hydrogen Phosphate API Price is not always fixed or binding as the Disodium Hydrogen Phosphate Price is obtained through a variety of data sources. The Disodium Hydrogen Phosphate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A OSMOPREP manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of OSMOPREP, including repackagers and relabelers. The FDA regulates OSMOPREP manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. OSMOPREP 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 OSMOPREP supplier is an individual or a company that provides OSMOPREP active pharmaceutical ingredient (API) or OSMOPREP finished formulations upon request. The OSMOPREP suppliers may include OSMOPREP API manufacturers, exporters, distributors and traders.
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A OSMOPREP written confirmation (OSMOPREP WC) is an official document issued by a regulatory agency to a OSMOPREP manufacturer, verifying that the manufacturing facility of a OSMOPREP active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting OSMOPREP APIs or OSMOPREP finished pharmaceutical products to another nation, regulatory agencies frequently require a OSMOPREP WC (written confirmation) as part of the regulatory process.
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