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01 1M/s Harman Finochem limited
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01 1Oxybutynin Chloride USP
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01 1WC-0045nA2
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01 1India
Date of Issue : 2022-08-06
Valid Till : 2025-07-21
Written Confirmation Number : WC-0045nA2
Address of the Firm : Plot No. E-7, E-8, E-9, MIDC Industrial Area, Chikalthana, Aurangabad-431006
31
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PharmaCompass also assists you with knowing the Oxybutynin API Price utilized in the formulation of products. Oxybutynin API Price is not always fixed or binding as the Oxybutynin Price is obtained through a variety of data sources. The Oxybutynin Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Oxybutin Holsten manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Oxybutin Holsten, including repackagers and relabelers. The FDA regulates Oxybutin Holsten manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Oxybutin Holsten 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 Oxybutin Holsten supplier is an individual or a company that provides Oxybutin Holsten active pharmaceutical ingredient (API) or Oxybutin Holsten finished formulations upon request. The Oxybutin Holsten suppliers may include Oxybutin Holsten API manufacturers, exporters, distributors and traders.
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A Oxybutin Holsten written confirmation (Oxybutin Holsten WC) is an official document issued by a regulatory agency to a Oxybutin Holsten manufacturer, verifying that the manufacturing facility of a Oxybutin Holsten active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Oxybutin Holsten APIs or Oxybutin Holsten finished pharmaceutical products to another nation, regulatory agencies frequently require a Oxybutin Holsten WC (written confirmation) as part of the regulatory process.
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