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