01 1M/s Medinex Laboratories Pvt. Ltd
01 1Dimenhydrinate BP/EP/USP
01 1WC-0279
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.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Dimenhydrinate manufacturer or Dimenhydrinate supplier.
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 Vomisin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Vomisin, including repackagers and relabelers. The FDA regulates Vomisin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Vomisin 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 Vomisin supplier is an individual or a company that provides Vomisin active pharmaceutical ingredient (API) or Vomisin finished formulations upon request. The Vomisin suppliers may include Vomisin API manufacturers, exporters, distributors and traders.
click here to find a list of Vomisin suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Vomisin written confirmation (Vomisin WC) is an official document issued by a regulatory agency to a Vomisin manufacturer, verifying that the manufacturing facility of a Vomisin active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Vomisin APIs or Vomisin finished pharmaceutical products to another nation, regulatory agencies frequently require a Vomisin WC (written confirmation) as part of the regulatory process.
click here to find a list of Vomisin suppliers with Written Confirmation (WC) on PharmaCompass.
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