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. Apicore Pharmaceuticals Pvt. Ltd.,
01 1Cevimeline HCl IH
02 1Cevimeline Hydrochloride IHS
01 1WC-0110n
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 : 2022-07-15
Valid Till : 2025-07-02
Written Confirmation Number : WC-0110n
Address of the Firm : 252-253, Dhobikuva-391 440, Opp.Jain Irrigation, Padra Jambusar Highway, Tal.Pad...
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PharmaCompass offers a list of Cevimeline Hydrochloride API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, Price,and more, enabling you to easily find the right Cevimeline Hydrochloride manufacturer or Cevimeline Hydrochloride supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Cevimeline Hydrochloride manufacturer or Cevimeline Hydrochloride supplier.
PharmaCompass also assists you with knowing the Cevimeline Hydrochloride API Price utilized in the formulation of products. Cevimeline Hydrochloride API Price is not always fixed or binding as the Cevimeline Hydrochloride Price is obtained through a variety of data sources. The Cevimeline Hydrochloride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Cevimeline Hydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Cevimeline Hydrochloride, including repackagers and relabelers. The FDA regulates Cevimeline Hydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Cevimeline Hydrochloride API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
click here to find a list of Cevimeline Hydrochloride manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Cevimeline Hydrochloride supplier is an individual or a company that provides Cevimeline Hydrochloride active pharmaceutical ingredient (API) or Cevimeline Hydrochloride finished formulations upon request. The Cevimeline Hydrochloride suppliers may include Cevimeline Hydrochloride API manufacturers, exporters, distributors and traders.
click here to find a list of Cevimeline Hydrochloride suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Cevimeline Hydrochloride written confirmation (Cevimeline Hydrochloride WC) is an official document issued by a regulatory agency to a Cevimeline Hydrochloride manufacturer, verifying that the manufacturing facility of a Cevimeline Hydrochloride active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Cevimeline Hydrochloride APIs or Cevimeline Hydrochloride finished pharmaceutical products to another nation, regulatory agencies frequently require a Cevimeline Hydrochloride WC (written confirmation) as part of the regulatory process.
click here to find a list of Cevimeline Hydrochloride suppliers with Written Confirmation (WC) on PharmaCompass.
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