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API SUPPLIERS
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Rochem International Inc
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Pharm-RX Chemical
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USP
ABOUT THIS PAGE
A Sulfacetamide manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Sulfacetamide, including repackagers and relabelers. The FDA regulates Sulfacetamide manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Sulfacetamide 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 Sulfacetamide manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Sulfacetamide supplier is an individual or a company that provides Sulfacetamide active pharmaceutical ingredient (API) or Sulfacetamide finished formulations upon request. The Sulfacetamide suppliers may include Sulfacetamide API manufacturers, exporters, distributors and traders.
click here to find a list of Sulfacetamide suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Sulfacetamide DMF (Drug Master File) is a document detailing the whole manufacturing process of Sulfacetamide active pharmaceutical ingredient (API) in detail. Different forms of Sulfacetamide DMFs exist exist since differing nations have different regulations, such as Sulfacetamide USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Sulfacetamide DMF submitted to regulatory agencies in the US is known as a USDMF. Sulfacetamide USDMF includes data on Sulfacetamide's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Sulfacetamide USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Sulfacetamide suppliers with USDMF on PharmaCompass.
National Drug Code is a comprehensive database maintained by the FDA that contains information on all drugs marketed in the US. This directory includes information about finished drug products, unfinished drug products, and compounded drug products, including those containing Sulfacetamide as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Sulfacetamide API and other APIs are published in this directory by the FDA.
The NDC unfinished drugs database includes product listing information submitted for all unfinished drugs, such as active pharmaceutical ingredients (APIs), drugs intended for further processing and bulk drug substances for compounding.
Pharmaceutical companies that manufacture Sulfacetamide as an active pharmaceutical ingredient (API) must furnish the FDA with an updated record of all drugs that they produce, prepare, propagate, compound, or process for commercial distribution in the US at their facilities.
The NDC directory also contains data on finished compounded human drug products that contain Sulfacetamide and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Sulfacetamide NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Sulfacetamide suppliers with NDC on PharmaCompass.
Sulfacetamide 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 Sulfacetamide 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 Sulfacetamide GMP manufacturer or Sulfacetamide GMP API supplier for your needs.
A Sulfacetamide CoA (Certificate of Analysis) is a formal document that attests to Sulfacetamide's compliance with Sulfacetamide specifications and serves as a tool for batch-level quality control.
Sulfacetamide CoA mostly includes findings from lab analyses of a specific batch. For each Sulfacetamide 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.
Sulfacetamide may be tested according to a variety of international standards, such as European Pharmacopoeia (Sulfacetamide EP), Sulfacetamide JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Sulfacetamide USP).
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