01 1M/s Saurav Chemicals Ltd
01 1Loxoprofen sodium hydrate JP
01 1WC-0171
01 1India
Date of Issue : 2022-11-02
Valid Till : 2025-08-13
Written Confirmation Number : WC-0171
Address of the Firm : Deravassi- Barwala Road Village-Bhagwanpura, Teh Bhagwanpura, Derabassi, Dist- S...
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PharmaCompass offers a list of Loxoprofen Sodium 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 Loxoprofen Sodium manufacturer or Loxoprofen Sodium supplier for your needs.
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PharmaCompass also assists you with knowing the Loxoprofen Sodium API Price utilized in the formulation of products. Loxoprofen Sodium API Price is not always fixed or binding as the Loxoprofen Sodium Price is obtained through a variety of data sources. The Loxoprofen Sodium Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Oxeno manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Oxeno, including repackagers and relabelers. The FDA regulates Oxeno manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Oxeno 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 Oxeno manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Oxeno supplier is an individual or a company that provides Oxeno active pharmaceutical ingredient (API) or Oxeno finished formulations upon request. The Oxeno suppliers may include Oxeno API manufacturers, exporters, distributors and traders.
click here to find a list of Oxeno suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Oxeno written confirmation (Oxeno WC) is an official document issued by a regulatory agency to a Oxeno manufacturer, verifying that the manufacturing facility of a Oxeno active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Oxeno APIs or Oxeno finished pharmaceutical products to another nation, regulatory agencies frequently require a Oxeno WC (written confirmation) as part of the regulatory process.
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