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01 1M/s Biochemical and Synthetic Products Pvt Ltd
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01 1Sodium Amino Salicylate Dihydrate BP/Ph. Eur
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01 1WC-0274
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01 1India
Sodium Amino Salicylate Dihydrate BP/Ph. Eur
Date of Issue : 2024-07-31
Valid Till : 2027-01-01
Written Confirmation Number : WC-0274
Address of the Firm : Plot No. 11/6/2029, Phase-2, SVCIE (Sri Venkateshwara Corporation Industrial Est...
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PharmaCompass offers a list of 6018-19-5 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 6018-19-5 manufacturer or 6018-19-5 supplier for your needs.
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PharmaCompass also assists you with knowing the 6018-19-5 API Price utilized in the formulation of products. 6018-19-5 API Price is not always fixed or binding as the 6018-19-5 Price is obtained through a variety of data sources. The 6018-19-5 Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A 6018-19-5 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of 6018-19-5, including repackagers and relabelers. The FDA regulates 6018-19-5 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. 6018-19-5 API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
A 6018-19-5 supplier is an individual or a company that provides 6018-19-5 active pharmaceutical ingredient (API) or 6018-19-5 finished formulations upon request. The 6018-19-5 suppliers may include 6018-19-5 API manufacturers, exporters, distributors and traders.
click here to find a list of 6018-19-5 suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A 6018-19-5 written confirmation (6018-19-5 WC) is an official document issued by a regulatory agency to a 6018-19-5 manufacturer, verifying that the manufacturing facility of a 6018-19-5 active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting 6018-19-5 APIs or 6018-19-5 finished pharmaceutical products to another nation, regulatory agencies frequently require a 6018-19-5 WC (written confirmation) as part of the regulatory process.
click here to find a list of 6018-19-5 suppliers with Written Confirmation (WC) on PharmaCompass.
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