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