Supriya Lifesciences is a cGMP-compliant API manufacturing organization with a leadership position across key & niche products.
01 1M/s Supriya Lifesience Ltd
01 1Esketamine Hydrochloride BP/EP
01 1WC-0218
01 1India
Supriya Lifesciences is a cGMP-compliant API manufacturing organization with a leadership position across key & niche products.
Esketamine Hydrochloride BP/EP
Date of Issue : 2022-06-29
Valid Till : 2025-07-02
Written Confirmation Number : WC-0218
Address of the Firm : A-5/2, Late Parshuram Industrial Area, MIDC, Tal-Khed, Dist. Ratnagiri-415 722, ...
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PharmaCompass also assists you with knowing the Esketamine Hydrochloride API Price utilized in the formulation of products. Esketamine Hydrochloride API Price is not always fixed or binding as the Esketamine Hydrochloride Price is obtained through a variety of data sources. The Esketamine Hydrochloride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A (-)-Ketamine manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of (-)-Ketamine, including repackagers and relabelers. The FDA regulates (-)-Ketamine manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. (-)-Ketamine 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 (-)-Ketamine supplier is an individual or a company that provides (-)-Ketamine active pharmaceutical ingredient (API) or (-)-Ketamine finished formulations upon request. The (-)-Ketamine suppliers may include (-)-Ketamine API manufacturers, exporters, distributors and traders.
click here to find a list of (-)-Ketamine suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A (-)-Ketamine written confirmation ((-)-Ketamine WC) is an official document issued by a regulatory agency to a (-)-Ketamine manufacturer, verifying that the manufacturing facility of a (-)-Ketamine active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting (-)-Ketamine APIs or (-)-Ketamine finished pharmaceutical products to another nation, regulatory agencies frequently require a (-)-Ketamine WC (written confirmation) as part of the regulatory process.
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