01 1M/s Bakul Aromatics And Chemicals
01 1Theophylline Ethylenediamine Anhydrous EP
01 1WC-0480
01 1India
Theophylline Ethylenediamine Anhydrous EP
Date of Issue : 2024-03-21
Valid Till : 2026-07-15
Written Confirmation Number : WC-0480
Address of the Firm : A-6, MIDC, Patalganga Industrial Area, Kaire, Khalapur-410220 Dist. Raigad, Maha...
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PharmaCompass offers a list of Aminophylline 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 Aminophylline manufacturer or Aminophylline supplier for your needs.
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A Eufilina Venosa manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Eufilina Venosa, including repackagers and relabelers. The FDA regulates Eufilina Venosa manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Eufilina Venosa 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 Eufilina Venosa supplier is an individual or a company that provides Eufilina Venosa active pharmaceutical ingredient (API) or Eufilina Venosa finished formulations upon request. The Eufilina Venosa suppliers may include Eufilina Venosa API manufacturers, exporters, distributors and traders.
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A Eufilina Venosa written confirmation (Eufilina Venosa WC) is an official document issued by a regulatory agency to a Eufilina Venosa manufacturer, verifying that the manufacturing facility of a Eufilina Venosa active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Eufilina Venosa APIs or Eufilina Venosa finished pharmaceutical products to another nation, regulatory agencies frequently require a Eufilina Venosa WC (written confirmation) as part of the regulatory process.
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