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API SUPPLIERS
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USDMF
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Dr. Paul Lohmann® provides premium mineral salts backed by 140+ years of innovation, quality manufacturing, and global expertise.
Certificate Number : CEP 2004-232 - Rev 04
Status : Valid
Issue Date : 2025-01-21
Type : Chemical
Substance Number : 902
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Jai Radhe Sales is your partner for all your sourcing needs.
About the Company : Jai Radhe Sales, founded in 1999, is a global distributor specializing in high-quality pharmaceutical ingredients from India. It offers complete sourcing solutions, technical and r...
Pharm-Rx is a reputed global importer and distributor of pharmaceutical active ingredients.
About the Company : Established in 1991, Pharm-Rx is an importer and distributor of active ingredients serving the pharmaceutical, nutritional supplement, and food industries. The company follows a hi...
Tenatra connects Indian manufacturers with global buyers through active partners in Germany, Switzerland, Belgium, Spain & Turkey.
About the Company : Tenatra International was established as a proprietorship firm in 1999. It got off to a very good start, supporting clients in the United States, Mexico and Europe. As business opp...
Dr. Paul Lohmann® provides premium mineral salts backed by 140+ years of innovation, quality manufacturing, and global expertise.
About the Company : Dr. Paul Lohmann® is a Germany based developer & manufacturer of high quality mineral salts with over 140 years of expertise. The company offers more than 400 salts in over 7,000 ...
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REF. STANDARDS & IMPURITIES
ABOUT THIS PAGE
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PharmaCompass offers a list of Ferrous Fumarate API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, and more, enabling you to easily find the right Ferrous Fumarate manufacturer or Ferrous Fumarate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Ferrous Fumarate manufacturer or Ferrous Fumarate supplier.
A Ferrocap manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Ferrocap, including repackagers and relabelers. The FDA regulates Ferrocap manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Ferrocap 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 Ferrocap manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A Ferrocap supplier is an individual or a company that provides Ferrocap active pharmaceutical ingredient (API) or Ferrocap finished formulations upon request. The Ferrocap suppliers may include Ferrocap API manufacturers, exporters, distributors and traders.
click here to find a list of Ferrocap suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PharmaCompass.
A Ferrocap DMF (Drug Master File) is a document detailing the whole manufacturing process of Ferrocap active pharmaceutical ingredient (API) in detail. Different forms of Ferrocap DMFs exist exist since differing nations have different regulations, such as Ferrocap USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Ferrocap DMF submitted to regulatory agencies in the US is known as a USDMF. Ferrocap USDMF includes data on Ferrocap's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Ferrocap USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Ferrocap suppliers with USDMF on PharmaCompass.
A Ferrocap CEP of the European Pharmacopoeia monograph is often referred to as a Ferrocap Certificate of Suitability (COS). The purpose of a Ferrocap CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Ferrocap EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Ferrocap to their clients by showing that a Ferrocap CEP has been issued for it. The manufacturer submits a Ferrocap CEP (COS) as part of the market authorization procedure, and it takes on the role of a Ferrocap CEP holder for the record. Additionally, the data presented in the Ferrocap CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Ferrocap DMF.
A Ferrocap CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Ferrocap 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 Ferrocap 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 Ferrocap as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Ferrocap 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 Ferrocap 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 Ferrocap and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Ferrocap NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Ferrocap suppliers with NDC on PharmaCompass.
Ferrocap 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 Ferrocap GMP manufacturers, exporters & distributors, which can be sorted by USDMF, JDMF, KDMF, CEP (COS), WC, and more, enabling you to easily find the right Ferrocap GMP manufacturer or Ferrocap GMP API supplier for your needs.
A Ferrocap CoA (Certificate of Analysis) is a formal document that attests to Ferrocap's compliance with Ferrocap specifications and serves as a tool for batch-level quality control.
Ferrocap CoA mostly includes findings from lab analyses of a specific batch. For each Ferrocap 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.
Ferrocap may be tested according to a variety of international standards, such as European Pharmacopoeia (Ferrocap EP), Ferrocap JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Ferrocap USP).
