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