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01 1M/s Medinex Laboratories Pvt. Ltd
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01 1Dimenhydrinate BP/EP/USP
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01 1WC-0279
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01 1India
Date of Issue : 2021-10-05
Valid Till : 2024-06-24
Written Confirmation Number : WC-0279
Address of the Firm : Plot No. 2 & 3, Survey No. 277/1, Block No. 177/1, Village: Ukhrala-364005, Tehs...
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PharmaCompass offers a list of Dimenhydrinate 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 Dimenhydrinate manufacturer or Dimenhydrinate supplier for your needs.
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PharmaCompass also assists you with knowing the Dimenhydrinate API Price utilized in the formulation of products. Dimenhydrinate API Price is not always fixed or binding as the Dimenhydrinate Price is obtained through a variety of data sources. The Dimenhydrinate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Reisetabletten ratiopharm manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Reisetabletten ratiopharm, including repackagers and relabelers. The FDA regulates Reisetabletten ratiopharm manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Reisetabletten ratiopharm 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 Reisetabletten ratiopharm supplier is an individual or a company that provides Reisetabletten ratiopharm active pharmaceutical ingredient (API) or Reisetabletten ratiopharm finished formulations upon request. The Reisetabletten ratiopharm suppliers may include Reisetabletten ratiopharm API manufacturers, exporters, distributors and traders.
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A Reisetabletten ratiopharm written confirmation (Reisetabletten ratiopharm WC) is an official document issued by a regulatory agency to a Reisetabletten ratiopharm manufacturer, verifying that the manufacturing facility of a Reisetabletten ratiopharm active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Reisetabletten ratiopharm APIs or Reisetabletten ratiopharm finished pharmaceutical products to another nation, regulatory agencies frequently require a Reisetabletten ratiopharm WC (written confirmation) as part of the regulatory process.
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