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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PharmaCompass also assists you with knowing the Aminophylline API Price utilized in the formulation of products. Aminophylline API Price is not always fixed or binding as the Aminophylline Price is obtained through a variety of data sources. The Aminophylline Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Syntophyllin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Syntophyllin, including repackagers and relabelers. The FDA regulates Syntophyllin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Syntophyllin 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 Syntophyllin supplier is an individual or a company that provides Syntophyllin active pharmaceutical ingredient (API) or Syntophyllin finished formulations upon request. The Syntophyllin suppliers may include Syntophyllin API manufacturers, exporters, distributors and traders.
click here to find a list of Syntophyllin suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Syntophyllin written confirmation (Syntophyllin WC) is an official document issued by a regulatory agency to a Syntophyllin manufacturer, verifying that the manufacturing facility of a Syntophyllin active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Syntophyllin APIs or Syntophyllin finished pharmaceutical products to another nation, regulatory agencies frequently require a Syntophyllin WC (written confirmation) as part of the regulatory process.
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