01 1M/s Azico Biophore India pvt Ltd
01 1Procainamide Hydrochloride USP/Ph.Eur.
01 1WC-0404
01 1India
Procainamide Hydrochloride USP/Ph.Eur.
Date of Issue : 2023-11-15
Valid Till : 2026-11-14
Written Confirmation Number : WC-0404
Address of the Firm : Plot No. 40/A, Sy Nos. 13,15,16,51,52 & 182, J.N. Pharma city, Thanam Village, P...
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PharmaCompass offers a list of Procainamide 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 Procainamide Hydrochloride manufacturer or Procainamide Hydrochloride supplier for your needs.
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PharmaCompass also assists you with knowing the Procainamide Hydrochloride API Price utilized in the formulation of products. Procainamide Hydrochloride API Price is not always fixed or binding as the Procainamide Hydrochloride Price is obtained through a variety of data sources. The Procainamide Hydrochloride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Pronestyl manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Pronestyl, including repackagers and relabelers. The FDA regulates Pronestyl manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Pronestyl 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 Pronestyl supplier is an individual or a company that provides Pronestyl active pharmaceutical ingredient (API) or Pronestyl finished formulations upon request. The Pronestyl suppliers may include Pronestyl API manufacturers, exporters, distributors and traders.
click here to find a list of Pronestyl suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Pronestyl written confirmation (Pronestyl WC) is an official document issued by a regulatory agency to a Pronestyl manufacturer, verifying that the manufacturing facility of a Pronestyl active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Pronestyl APIs or Pronestyl finished pharmaceutical products to another nation, regulatory agencies frequently require a Pronestyl WC (written confirmation) as part of the regulatory process.
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