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PharmaCompass offers a list of Sodium Fluoride 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 Fluoride manufacturer or Sodium Fluoride supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Sodium Fluoride manufacturer or Sodium Fluoride supplier.
PharmaCompass also assists you with knowing the Sodium Fluoride API Price utilized in the formulation of products. Sodium Fluoride API Price is not always fixed or binding as the Sodium Fluoride Price is obtained through a variety of data sources. The Sodium Fluoride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A 01148_RIEDEL manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of 01148_RIEDEL, including repackagers and relabelers. The FDA regulates 01148_RIEDEL manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. 01148_RIEDEL 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 01148_RIEDEL manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A 01148_RIEDEL supplier is an individual or a company that provides 01148_RIEDEL active pharmaceutical ingredient (API) or 01148_RIEDEL finished formulations upon request. The 01148_RIEDEL suppliers may include 01148_RIEDEL API manufacturers, exporters, distributors and traders.
click here to find a list of 01148_RIEDEL suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A 01148_RIEDEL DMF (Drug Master File) is a document detailing the whole manufacturing process of 01148_RIEDEL active pharmaceutical ingredient (API) in detail. Different forms of 01148_RIEDEL DMFs exist exist since differing nations have different regulations, such as 01148_RIEDEL USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A 01148_RIEDEL DMF submitted to regulatory agencies in the US is known as a USDMF. 01148_RIEDEL USDMF includes data on 01148_RIEDEL's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The 01148_RIEDEL USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of 01148_RIEDEL suppliers with USDMF on PharmaCompass.
A 01148_RIEDEL CEP of the European Pharmacopoeia monograph is often referred to as a 01148_RIEDEL Certificate of Suitability (COS). The purpose of a 01148_RIEDEL CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of 01148_RIEDEL EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of 01148_RIEDEL to their clients by showing that a 01148_RIEDEL CEP has been issued for it. The manufacturer submits a 01148_RIEDEL CEP (COS) as part of the market authorization procedure, and it takes on the role of a 01148_RIEDEL CEP holder for the record. Additionally, the data presented in the 01148_RIEDEL CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the 01148_RIEDEL DMF.
A 01148_RIEDEL CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. 01148_RIEDEL 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 01148_RIEDEL 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 01148_RIEDEL as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for 01148_RIEDEL 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 01148_RIEDEL 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 01148_RIEDEL and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a 01148_RIEDEL NDC to their finished compounded human drug products, they may choose to do so.
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01148_RIEDEL 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 01148_RIEDEL 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 01148_RIEDEL GMP manufacturer or 01148_RIEDEL GMP API supplier for your needs.
A 01148_RIEDEL CoA (Certificate of Analysis) is a formal document that attests to 01148_RIEDEL's compliance with 01148_RIEDEL specifications and serves as a tool for batch-level quality control.
01148_RIEDEL CoA mostly includes findings from lab analyses of a specific batch. For each 01148_RIEDEL 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.
01148_RIEDEL may be tested according to a variety of international standards, such as European Pharmacopoeia (01148_RIEDEL EP), 01148_RIEDEL JP (Japanese Pharmacopeia) and the US Pharmacopoeia (01148_RIEDEL USP).
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