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PharmaCompass offers a list of Sodium Sulfate 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 Sodium Sulfate manufacturer or Sodium Sulfate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Sodium Sulfate manufacturer or Sodium Sulfate supplier.
PharmaCompass also assists you with knowing the Sodium Sulfate API Price utilized in the formulation of products. Sodium Sulfate API Price is not always fixed or binding as the Sodium Sulfate Price is obtained through a variety of data sources. The Sodium Sulfate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A SODIUM SULFATE ANHYDROUS manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of SODIUM SULFATE ANHYDROUS, including repackagers and relabelers. The FDA regulates SODIUM SULFATE ANHYDROUS manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. SODIUM SULFATE ANHYDROUS 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 SODIUM SULFATE ANHYDROUS manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A SODIUM SULFATE ANHYDROUS supplier is an individual or a company that provides SODIUM SULFATE ANHYDROUS active pharmaceutical ingredient (API) or SODIUM SULFATE ANHYDROUS finished formulations upon request. The SODIUM SULFATE ANHYDROUS suppliers may include SODIUM SULFATE ANHYDROUS API manufacturers, exporters, distributors and traders.
click here to find a list of SODIUM SULFATE ANHYDROUS suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A SODIUM SULFATE ANHYDROUS DMF (Drug Master File) is a document detailing the whole manufacturing process of SODIUM SULFATE ANHYDROUS active pharmaceutical ingredient (API) in detail. Different forms of SODIUM SULFATE ANHYDROUS DMFs exist exist since differing nations have different regulations, such as SODIUM SULFATE ANHYDROUS USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A SODIUM SULFATE ANHYDROUS DMF submitted to regulatory agencies in the US is known as a USDMF. SODIUM SULFATE ANHYDROUS USDMF includes data on SODIUM SULFATE ANHYDROUS's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The SODIUM SULFATE ANHYDROUS USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of SODIUM SULFATE ANHYDROUS suppliers with USDMF on PharmaCompass.
The Pharmaceuticals and Medical Devices Agency (PMDA) established the Japan Drug Master File (JDMF), also known as the Master File (MF), to permit Japanese and foreign manufacturers of drug substances, intermediates, excipients, raw materials, and packaging materials (‘Products’) to voluntarily register confidential information about the production and management of their products in Japan.
The SODIUM SULFATE ANHYDROUS Drug Master File in Japan (SODIUM SULFATE ANHYDROUS JDMF) empowers SODIUM SULFATE ANHYDROUS API manufacturers to present comprehensive information (e.g., production methods, data, etc.) to the review authority, i.e., PMDA (Pharmaceuticals & Medical Devices Agency).
PMDA reviews the SODIUM SULFATE ANHYDROUS JDMF during the approval evaluation for pharmaceutical products. At the time of SODIUM SULFATE ANHYDROUS JDMF registration, PMDA checks if the format is accurate, if the necessary items have been included (application), and if data has been attached.
click here to find a list of SODIUM SULFATE ANHYDROUS suppliers with JDMF on PharmaCompass.
A SODIUM SULFATE ANHYDROUS CEP of the European Pharmacopoeia monograph is often referred to as a SODIUM SULFATE ANHYDROUS Certificate of Suitability (COS). The purpose of a SODIUM SULFATE ANHYDROUS CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of SODIUM SULFATE ANHYDROUS EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of SODIUM SULFATE ANHYDROUS to their clients by showing that a SODIUM SULFATE ANHYDROUS CEP has been issued for it. The manufacturer submits a SODIUM SULFATE ANHYDROUS CEP (COS) as part of the market authorization procedure, and it takes on the role of a SODIUM SULFATE ANHYDROUS CEP holder for the record. Additionally, the data presented in the SODIUM SULFATE ANHYDROUS CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the SODIUM SULFATE ANHYDROUS DMF.
A SODIUM SULFATE ANHYDROUS CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. SODIUM SULFATE ANHYDROUS CEPs may be accepted in nations that are not members of the Ph. Eur. at the discretion of the authorities there.
click here to find a list of SODIUM SULFATE ANHYDROUS suppliers with CEP (COS) 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 SODIUM SULFATE ANHYDROUS as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for SODIUM SULFATE ANHYDROUS 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 SODIUM SULFATE ANHYDROUS 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 SODIUM SULFATE ANHYDROUS and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a SODIUM SULFATE ANHYDROUS NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of SODIUM SULFATE ANHYDROUS suppliers with NDC on PharmaCompass.
SODIUM SULFATE ANHYDROUS 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 SODIUM SULFATE ANHYDROUS 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 SODIUM SULFATE ANHYDROUS GMP manufacturer or SODIUM SULFATE ANHYDROUS GMP API supplier for your needs.
A SODIUM SULFATE ANHYDROUS CoA (Certificate of Analysis) is a formal document that attests to SODIUM SULFATE ANHYDROUS's compliance with SODIUM SULFATE ANHYDROUS specifications and serves as a tool for batch-level quality control.
SODIUM SULFATE ANHYDROUS CoA mostly includes findings from lab analyses of a specific batch. For each SODIUM SULFATE ANHYDROUS 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.
SODIUM SULFATE ANHYDROUS may be tested according to a variety of international standards, such as European Pharmacopoeia (SODIUM SULFATE ANHYDROUS EP), SODIUM SULFATE ANHYDROUS JP (Japanese Pharmacopeia) and the US Pharmacopoeia (SODIUM SULFATE ANHYDROUS USP).
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