01 1M/s. Dishman Pharmaceuticals and Chemicals Ltd.
01 1Etofenamate Ph.Eur
01 1WC-0135
01 1India
Date of Issue : 2019-07-22
Valid Till : 2022-07-02
Written Confirmation Number : WC-0135
Address of the Firm : Survey No. 47, Paiki Sub Plot No. 1, Village Lodariyal, Taluka Sanand, Dist. Ahm...
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PharmaCompass offers a list of Etofenamate 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 Etofenamate manufacturer or Etofenamate supplier for your needs.
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PharmaCompass also assists you with knowing the Etofenamate API Price utilized in the formulation of products. Etofenamate API Price is not always fixed or binding as the Etofenamate Price is obtained through a variety of data sources. The Etofenamate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Rheumon gel manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Rheumon gel, including repackagers and relabelers. The FDA regulates Rheumon gel manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Rheumon gel 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 Rheumon gel supplier is an individual or a company that provides Rheumon gel active pharmaceutical ingredient (API) or Rheumon gel finished formulations upon request. The Rheumon gel suppliers may include Rheumon gel API manufacturers, exporters, distributors and traders.
click here to find a list of Rheumon gel suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Rheumon gel written confirmation (Rheumon gel WC) is an official document issued by a regulatory agency to a Rheumon gel manufacturer, verifying that the manufacturing facility of a Rheumon gel active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Rheumon gel APIs or Rheumon gel finished pharmaceutical products to another nation, regulatory agencies frequently require a Rheumon gel WC (written confirmation) as part of the regulatory process.
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