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ABOUT THIS PAGE
A Sodium Hydrogenphosphate Dihydrate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Sodium Hydrogenphosphate Dihydrate, including repackagers and relabelers. The FDA regulates Sodium Hydrogenphosphate Dihydrate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Sodium Hydrogenphosphate Dihydrate 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 Hydrogenphosphate Dihydrate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Sodium Hydrogenphosphate Dihydrate supplier is an individual or a company that provides Sodium Hydrogenphosphate Dihydrate active pharmaceutical ingredient (API) or Sodium Hydrogenphosphate Dihydrate finished formulations upon request. The Sodium Hydrogenphosphate Dihydrate suppliers may include Sodium Hydrogenphosphate Dihydrate API manufacturers, exporters, distributors and traders.
click here to find a list of Sodium Hydrogenphosphate Dihydrate suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Sodium Hydrogenphosphate Dihydrate DMF (Drug Master File) is a document detailing the whole manufacturing process of Sodium Hydrogenphosphate Dihydrate active pharmaceutical ingredient (API) in detail. Different forms of Sodium Hydrogenphosphate Dihydrate DMFs exist exist since differing nations have different regulations, such as Sodium Hydrogenphosphate Dihydrate USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Sodium Hydrogenphosphate Dihydrate DMF submitted to regulatory agencies in the US is known as a USDMF. Sodium Hydrogenphosphate Dihydrate USDMF includes data on Sodium Hydrogenphosphate Dihydrate's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Sodium Hydrogenphosphate Dihydrate USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Sodium Hydrogenphosphate Dihydrate 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 Sodium Hydrogenphosphate Dihydrate as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Sodium Hydrogenphosphate Dihydrate 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 Hydrogenphosphate Dihydrate 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 Hydrogenphosphate Dihydrate and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Sodium Hydrogenphosphate Dihydrate NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Sodium Hydrogenphosphate Dihydrate suppliers with NDC on PharmaCompass.
Sodium Hydrogenphosphate Dihydrate 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 Hydrogenphosphate Dihydrate 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 Hydrogenphosphate Dihydrate GMP manufacturer or Sodium Hydrogenphosphate Dihydrate GMP API supplier for your needs.
A Sodium Hydrogenphosphate Dihydrate CoA (Certificate of Analysis) is a formal document that attests to Sodium Hydrogenphosphate Dihydrate's compliance with Sodium Hydrogenphosphate Dihydrate specifications and serves as a tool for batch-level quality control.
Sodium Hydrogenphosphate Dihydrate CoA mostly includes findings from lab analyses of a specific batch. For each Sodium Hydrogenphosphate Dihydrate 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 Hydrogenphosphate Dihydrate may be tested according to a variety of international standards, such as European Pharmacopoeia (Sodium Hydrogenphosphate Dihydrate EP), Sodium Hydrogenphosphate Dihydrate JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Sodium Hydrogenphosphate Dihydrate USP).
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