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01 1M/s. Macleods Pharmaceuticals Ltd.
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01 1lndomethacin (Ph. Eur./USP)
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01 1WC-0079
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01 1India
Date of Issue : 2019-11-28
Valid Till : 2022-07-02
Written Confirmation Number : WC-0079
Address of the Firm : Plot No.2209, GIDC, Industrial Estate, At & Post Sarigam, Tal-Umbergaon, Valsad-...
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PharmaCompass offers a list of Indomethacin 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 Indomethacin manufacturer or Indomethacin supplier for your needs.
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PharmaCompass also assists you with knowing the Indomethacin API Price utilized in the formulation of products. Indomethacin API Price is not always fixed or binding as the Indomethacin Price is obtained through a variety of data sources. The Indomethacin Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A TIVORBEX manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of TIVORBEX, including repackagers and relabelers. The FDA regulates TIVORBEX manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. TIVORBEX 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 TIVORBEX supplier is an individual or a company that provides TIVORBEX active pharmaceutical ingredient (API) or TIVORBEX finished formulations upon request. The TIVORBEX suppliers may include TIVORBEX API manufacturers, exporters, distributors and traders.
click here to find a list of TIVORBEX suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A TIVORBEX written confirmation (TIVORBEX WC) is an official document issued by a regulatory agency to a TIVORBEX manufacturer, verifying that the manufacturing facility of a TIVORBEX active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting TIVORBEX APIs or TIVORBEX finished pharmaceutical products to another nation, regulatory agencies frequently require a TIVORBEX WC (written confirmation) as part of the regulatory process.
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