01 1M/s Aurore Pharmaceutical Private Limited
01 1valaciclovir Hydrochloride Hydrated BP/EP
01 1WC-0119A6
01 1India
valaciclovir Hydrochloride Hydrated BP/EP
Date of Issue : 2020-08-07
Valid Till : 2022-07-02
Written Confirmation Number : WC-0119A6
Address of the Firm : Plot No. 35, 36, 38, 39, 40, 49, 50, & 51, Phase IV, IDA, Jeedimetla, Medchal-Ma...
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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 Zelitrex manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Zelitrex, including repackagers and relabelers. The FDA regulates Zelitrex manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Zelitrex 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 Zelitrex supplier is an individual or a company that provides Zelitrex active pharmaceutical ingredient (API) or Zelitrex finished formulations upon request. The Zelitrex suppliers may include Zelitrex API manufacturers, exporters, distributors and traders.
click here to find a list of Zelitrex suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Zelitrex written confirmation (Zelitrex WC) is an official document issued by a regulatory agency to a Zelitrex manufacturer, verifying that the manufacturing facility of a Zelitrex active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Zelitrex APIs or Zelitrex finished pharmaceutical products to another nation, regulatory agencies frequently require a Zelitrex WC (written confirmation) as part of the regulatory process.
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