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01 1M/s Aurore Pharmaceuticals Private Limited
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01 1Erdosteine IH
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01 1WC-0119
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01 1India
Date of Issue : 2022-09-19
Valid Till : 2025-07-02
Written Confirmation Number : WC-0119
Address of the Firm : Plot No. 35, 36, 38, 39,40,49, 50 & 51, Phase-IV, IDA, Jeedimetla, Medchal- Malk...
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PharmaCompass offers a list of Erdosteine 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 Erdosteine manufacturer or Erdosteine supplier for your needs.
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PharmaCompass also assists you with knowing the Erdosteine API Price utilized in the formulation of products. Erdosteine API Price is not always fixed or binding as the Erdosteine Price is obtained through a variety of data sources. The Erdosteine Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Vectrine manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Vectrine, including repackagers and relabelers. The FDA regulates Vectrine manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Vectrine 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 Vectrine manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Vectrine supplier is an individual or a company that provides Vectrine active pharmaceutical ingredient (API) or Vectrine finished formulations upon request. The Vectrine suppliers may include Vectrine API manufacturers, exporters, distributors and traders.
click here to find a list of Vectrine suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Vectrine written confirmation (Vectrine WC) is an official document issued by a regulatory agency to a Vectrine manufacturer, verifying that the manufacturing facility of a Vectrine active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Vectrine APIs or Vectrine finished pharmaceutical products to another nation, regulatory agencies frequently require a Vectrine WC (written confirmation) as part of the regulatory process.
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