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PharmaCompass offers a list of Theophylline Sodium Glycinate 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 Theophylline Sodium Glycinate manufacturer or Theophylline Sodium Glycinate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Theophylline Sodium Glycinate manufacturer or Theophylline Sodium Glycinate supplier.
PharmaCompass also assists you with knowing the Theophylline Sodium Glycinate API Price utilized in the formulation of products. Theophylline Sodium Glycinate API Price is not always fixed or binding as the Theophylline Sodium Glycinate Price is obtained through a variety of data sources. The Theophylline Sodium Glycinate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Slo-Phyllin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Slo-Phyllin, including repackagers and relabelers. The FDA regulates Slo-Phyllin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Slo-Phyllin 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 Slo-Phyllin manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Slo-Phyllin supplier is an individual or a company that provides Slo-Phyllin active pharmaceutical ingredient (API) or Slo-Phyllin finished formulations upon request. The Slo-Phyllin suppliers may include Slo-Phyllin API manufacturers, exporters, distributors and traders.
click here to find a list of Slo-Phyllin suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Slo-Phyllin DMF (Drug Master File) is a document detailing the whole manufacturing process of Slo-Phyllin active pharmaceutical ingredient (API) in detail. Different forms of Slo-Phyllin DMFs exist exist since differing nations have different regulations, such as Slo-Phyllin USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Slo-Phyllin DMF submitted to regulatory agencies in the US is known as a USDMF. Slo-Phyllin USDMF includes data on Slo-Phyllin's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Slo-Phyllin USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Slo-Phyllin suppliers with USDMF on PharmaCompass.
A Slo-Phyllin written confirmation (Slo-Phyllin WC) is an official document issued by a regulatory agency to a Slo-Phyllin manufacturer, verifying that the manufacturing facility of a Slo-Phyllin active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Slo-Phyllin APIs or Slo-Phyllin finished pharmaceutical products to another nation, regulatory agencies frequently require a Slo-Phyllin WC (written confirmation) as part of the regulatory process.
click here to find a list of Slo-Phyllin suppliers with Written Confirmation (WC) on PharmaCompass.
Slo-Phyllin Active pharmaceutical ingredient (API) is produced in GMP-certified manufacturing facility.
GMP stands for Good Manufacturing Practices, which is a system used in the pharmaceutical industry to make sure that goods are regularly produced and monitored in accordance with quality standards. The FDA’s current Good Manufacturing Practices requirements are referred to as cGMP or current GMP which indicates that the company follows the most recent GMP specifications. The World Health Organization (WHO) has its own set of GMP guidelines, called the WHO GMP. Different countries can also set their own guidelines for GMP like China (Chinese GMP) or the EU (EU GMP).
PharmaCompass offers a list of Slo-Phyllin GMP manufacturers, exporters & distributors, which can be sorted by USDMF, JDMF, KDMF, CEP (COS), WC, API price, and more, enabling you to easily find the right Slo-Phyllin GMP manufacturer or Slo-Phyllin GMP API supplier for your needs.
A Slo-Phyllin CoA (Certificate of Analysis) is a formal document that attests to Slo-Phyllin's compliance with Slo-Phyllin specifications and serves as a tool for batch-level quality control.
Slo-Phyllin CoA mostly includes findings from lab analyses of a specific batch. For each Slo-Phyllin CoA document that a company creates, the USFDA specifies specific requirements, such as supplier information, material identification, transportation data, evidence of conformity and signature data.
Slo-Phyllin may be tested according to a variety of international standards, such as European Pharmacopoeia (Slo-Phyllin EP), Slo-Phyllin JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Slo-Phyllin USP).
