01 1M/s Aurore Pharmaceuticals Private limited
01 1Valaciclovir Hydrochloride Hydrated Ph.Eur
01 1WC-0119
01 1India
Valaciclovir Hydrochloride Hydrated Ph.Eur
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-Mal...
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PharmaCompass offers a list of Valacyclovir 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 Valacyclovir manufacturer or Valacyclovir supplier for your needs.
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PharmaCompass also assists you with knowing the Valacyclovir API Price utilized in the formulation of products. Valacyclovir API Price is not always fixed or binding as the Valacyclovir Price is obtained through a variety of data sources. The Valacyclovir Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Viropel manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Viropel, including repackagers and relabelers. The FDA regulates Viropel manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Viropel 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 Viropel supplier is an individual or a company that provides Viropel active pharmaceutical ingredient (API) or Viropel finished formulations upon request. The Viropel suppliers may include Viropel API manufacturers, exporters, distributors and traders.
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A Viropel written confirmation (Viropel WC) is an official document issued by a regulatory agency to a Viropel manufacturer, verifying that the manufacturing facility of a Viropel active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Viropel APIs or Viropel finished pharmaceutical products to another nation, regulatory agencies frequently require a Viropel WC (written confirmation) as part of the regulatory process.
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