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01 1M/s. Mac-Chem Products (India) Pvt. Ltd
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01 1Tenoxicam BP
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01 1WC-0275
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01 1India
Date of Issue : 2021-01-22
Valid Till : 2023-08-01
Written Confirmation Number : WC-0275
Address of the Firm : N-211/2/10, MIDC, Boisar, Dist-Thane-401506, Mahrashtra
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PharmaCompass offers a list of Tenoxicam 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 Tenoxicam manufacturer or Tenoxicam supplier for your needs.
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PharmaCompass also assists you with knowing the Tenoxicam API Price utilized in the formulation of products. Tenoxicam API Price is not always fixed or binding as the Tenoxicam Price is obtained through a variety of data sources. The Tenoxicam Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Reutenox manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Reutenox, including repackagers and relabelers. The FDA regulates Reutenox manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Reutenox API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
click here to find a list of Reutenox manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Reutenox supplier is an individual or a company that provides Reutenox active pharmaceutical ingredient (API) or Reutenox finished formulations upon request. The Reutenox suppliers may include Reutenox API manufacturers, exporters, distributors and traders.
click here to find a list of Reutenox suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Reutenox written confirmation (Reutenox WC) is an official document issued by a regulatory agency to a Reutenox manufacturer, verifying that the manufacturing facility of a Reutenox active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Reutenox APIs or Reutenox finished pharmaceutical products to another nation, regulatory agencies frequently require a Reutenox WC (written confirmation) as part of the regulatory process.
click here to find a list of Reutenox suppliers with Written Confirmation (WC) on PharmaCompass.
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