Nuray is an expert in the synthesis of Niche novel APIs, the first to launch Generics, NCEs, Advanced Intermediates // USFDA certified.
01 1M/s Nuray Chemicals Private Limited
01 1Fludrocortisone Acetate USP
01 1WC-0416
01 1India
Nuray is an expert in the synthesis of Niche novel APIs, the first to launch Generics, NCEs, Advanced Intermediates // USFDA certified.
Date of Issue : 2024-02-20
Valid Till : 2026-12-06
Written Confirmation Number : WC-0416
Address of the Firm : Plot No. 111, SIDCO Industrial Estate, Kakkalur, Thiruvallur 602 003, Tamil Nadu...
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PharmaCompass also assists you with knowing the Fludrocortisone Acetate API Price utilized in the formulation of products. Fludrocortisone Acetate API Price is not always fixed or binding as the Fludrocortisone Acetate Price is obtained through a variety of data sources. The Fludrocortisone Acetate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Florinef acetate (TN) manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Florinef acetate (TN), including repackagers and relabelers. The FDA regulates Florinef acetate (TN) manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Florinef acetate (TN) 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 Florinef acetate (TN) supplier is an individual or a company that provides Florinef acetate (TN) active pharmaceutical ingredient (API) or Florinef acetate (TN) finished formulations upon request. The Florinef acetate (TN) suppliers may include Florinef acetate (TN) API manufacturers, exporters, distributors and traders.
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A Florinef acetate (TN) written confirmation (Florinef acetate (TN) WC) is an official document issued by a regulatory agency to a Florinef acetate (TN) manufacturer, verifying that the manufacturing facility of a Florinef acetate (TN) active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Florinef acetate (TN) APIs or Florinef acetate (TN) finished pharmaceutical products to another nation, regulatory agencies frequently require a Florinef acetate (TN) WC (written confirmation) as part of the regulatory process.
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