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 Pvt Ltd.,
02 1M/s Aurore Pharmaceuticals Private Limited
01 2Prazosin Hydrochloride USP
01 1WC-0119
02 1WC-0416
01 2India
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-602003 Tamil Nadu, In...
Date of Issue : 2022-09-19
Valid Till : 2025-07-02
Written Confirmation Number : WC-0119
Address of the Firm : Plot No. 35, 36, 38, 39,40,49, 50 & 51, Phase-IV, IDA, Jeedimetla, Medchal- Malk...
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PharmaCompass also assists you with knowing the Prazosin Hydrochloride API Price utilized in the formulation of products. Prazosin Hydrochloride API Price is not always fixed or binding as the Prazosin Hydrochloride Price is obtained through a variety of data sources. The Prazosin Hydrochloride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Vasoflex manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Vasoflex, including repackagers and relabelers. The FDA regulates Vasoflex manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Vasoflex 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 Vasoflex supplier is an individual or a company that provides Vasoflex active pharmaceutical ingredient (API) or Vasoflex finished formulations upon request. The Vasoflex suppliers may include Vasoflex API manufacturers, exporters, distributors and traders.
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A Vasoflex written confirmation (Vasoflex WC) is an official document issued by a regulatory agency to a Vasoflex manufacturer, verifying that the manufacturing facility of a Vasoflex active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Vasoflex APIs or Vasoflex finished pharmaceutical products to another nation, regulatory agencies frequently require a Vasoflex WC (written confirmation) as part of the regulatory process.
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