01 1M/sDy-Mach Pharma
01 1Sulphamethizole BP/USP
01 1WC-0410
01 1India
Date of Issue : 2021-03-12
Valid Till : 2024-03-04
Written Confirmation Number : WC-0410
Address of the Firm : C-1/2343-46 IIIrd Phase, G.I.D.C Vapi Dist. Valsad-396195 Gujarat India
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PharmaCompass offers a list of Sulfamethizole 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 Sulfamethizole manufacturer or Sulfamethizole supplier for your needs.
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PharmaCompass also assists you with knowing the Sulfamethizole API Price utilized in the formulation of products. Sulfamethizole API Price is not always fixed or binding as the Sulfamethizole Price is obtained through a variety of data sources. The Sulfamethizole Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Lucosil manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Lucosil, including repackagers and relabelers. The FDA regulates Lucosil manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Lucosil 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 Lucosil manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Lucosil supplier is an individual or a company that provides Lucosil active pharmaceutical ingredient (API) or Lucosil finished formulations upon request. The Lucosil suppliers may include Lucosil API manufacturers, exporters, distributors and traders.
click here to find a list of Lucosil suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Lucosil written confirmation (Lucosil WC) is an official document issued by a regulatory agency to a Lucosil manufacturer, verifying that the manufacturing facility of a Lucosil active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Lucosil APIs or Lucosil finished pharmaceutical products to another nation, regulatory agencies frequently require a Lucosil WC (written confirmation) as part of the regulatory process.
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