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