01 1M/s Suven Life Sciences Limited
01 1Thiabendazole USP/IH
01 1WC-0042N
01 1India
Date of Issue : 2022-08-16
Valid Till : 2025-07-15
Written Confirmation Number : WC-0042N
Address of the Firm : Plot Nos. 262 to 271, IDA, Pashamylaram, Sangareddy District- 502 307, Telangana...
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PharmaCompass offers a list of Thiabendazole 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 Thiabendazole manufacturer or Thiabendazole supplier for your needs.
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PharmaCompass also assists you with knowing the Thiabendazole API Price utilized in the formulation of products. Thiabendazole API Price is not always fixed or binding as the Thiabendazole Price is obtained through a variety of data sources. The Thiabendazole Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Helmindrax octelmin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Helmindrax octelmin, including repackagers and relabelers. The FDA regulates Helmindrax octelmin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Helmindrax octelmin 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 Helmindrax octelmin supplier is an individual or a company that provides Helmindrax octelmin active pharmaceutical ingredient (API) or Helmindrax octelmin finished formulations upon request. The Helmindrax octelmin suppliers may include Helmindrax octelmin API manufacturers, exporters, distributors and traders.
click here to find a list of Helmindrax octelmin suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Helmindrax octelmin written confirmation (Helmindrax octelmin WC) is an official document issued by a regulatory agency to a Helmindrax octelmin manufacturer, verifying that the manufacturing facility of a Helmindrax octelmin active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Helmindrax octelmin APIs or Helmindrax octelmin finished pharmaceutical products to another nation, regulatory agencies frequently require a Helmindrax octelmin WC (written confirmation) as part of the regulatory process.
click here to find a list of Helmindrax octelmin suppliers with Written Confirmation (WC) on PharmaCompass.
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