API Suppliers
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PharmaCompass offers a list of Sulfisoxazole 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 Sulfisoxazole manufacturer or Sulfisoxazole supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Sulfisoxazole manufacturer or Sulfisoxazole supplier.
PharmaCompass also assists you with knowing the Sulfisoxazole API Price utilized in the formulation of products. Sulfisoxazole API Price is not always fixed or binding as the Sulfisoxazole Price is obtained through a variety of data sources. The Sulfisoxazole Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Sulfisoxazole manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Sulfisoxazole, including repackagers and relabelers. The FDA regulates Sulfisoxazole manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Sulfisoxazole API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
A Sulfisoxazole supplier is an individual or a company that provides Sulfisoxazole active pharmaceutical ingredient (API) or Sulfisoxazole finished formulations upon request. The Sulfisoxazole suppliers may include Sulfisoxazole API manufacturers, exporters, distributors and traders.
click here to find a list of Sulfisoxazole suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Sulfisoxazole DMF (Drug Master File) is a document detailing the whole manufacturing process of Sulfisoxazole active pharmaceutical ingredient (API) in detail. Different forms of Sulfisoxazole DMFs exist exist since differing nations have different regulations, such as Sulfisoxazole USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Sulfisoxazole DMF submitted to regulatory agencies in the US is known as a USDMF. Sulfisoxazole USDMF includes data on Sulfisoxazole's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Sulfisoxazole USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Sulfisoxazole suppliers with USDMF on PharmaCompass.
Sulfisoxazole 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 Sulfisoxazole 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 Sulfisoxazole GMP manufacturer or Sulfisoxazole GMP API supplier for your needs.
A Sulfisoxazole CoA (Certificate of Analysis) is a formal document that attests to Sulfisoxazole's compliance with Sulfisoxazole specifications and serves as a tool for batch-level quality control.
Sulfisoxazole CoA mostly includes findings from lab analyses of a specific batch. For each Sulfisoxazole 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.
Sulfisoxazole may be tested according to a variety of international standards, such as European Pharmacopoeia (Sulfisoxazole EP), Sulfisoxazole JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Sulfisoxazole USP).