Nuray is an expert in the synthesis of Niche novel APIs, the first to launch Generics, NCEs, Advanced Intermediates // USFDA certified.
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01 1M/s Nuray Chemicals Private Limited
02 1M/sSri Krishna Phamaceuticals Ltd
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01 1Sodium Phenyl Butyrate Ph. Eur
02 1Sodium Phenylbutyrate IHS
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01 1WC-0033
02 1WC-0416
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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 ? 602 003, Tamil Na...
Sodium Phenyl Butyrate Ph. Eur
Date of Issue : 2022-06-20
Valid Till : 2025-07-28
Written Confirmation Number : WC-0033
Address of the Firm : Unit-III, Sy. No. 57, Golkonda Kalan, Raikunta Village, Shamshabad Mandai, Ranga...
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A S4125,1716-12-7 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of S4125,1716-12-7, including repackagers and relabelers. The FDA regulates S4125,1716-12-7 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. S4125,1716-12-7 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 S4125,1716-12-7 supplier is an individual or a company that provides S4125,1716-12-7 active pharmaceutical ingredient (API) or S4125,1716-12-7 finished formulations upon request. The S4125,1716-12-7 suppliers may include S4125,1716-12-7 API manufacturers, exporters, distributors and traders.
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A S4125,1716-12-7 written confirmation (S4125,1716-12-7 WC) is an official document issued by a regulatory agency to a S4125,1716-12-7 manufacturer, verifying that the manufacturing facility of a S4125,1716-12-7 active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting S4125,1716-12-7 APIs or S4125,1716-12-7 finished pharmaceutical products to another nation, regulatory agencies frequently require a S4125,1716-12-7 WC (written confirmation) as part of the regulatory process.
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