US DMFs Filed
USA (Orange Book)
PharmaCompass offers a list of Lanthanum Carbonate 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 Lanthanum Carbonate manufacturer or Lanthanum Carbonate supplier for your needs.
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PharmaCompass also assists you with knowing the Lanthanum Carbonate API Price utilized in the formulation of products. Lanthanum Carbonate API Price is not always fixed or binding as the Lanthanum Carbonate Price is obtained through a variety of data sources. The Lanthanum Carbonate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Lanthanum Carbonate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Lanthanum Carbonate, including repackagers and relabelers. The FDA regulates Lanthanum Carbonate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Lanthanum Carbonate API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
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A Lanthanum Carbonate supplier is an individual or a company that provides Lanthanum Carbonate active pharmaceutical ingredient (API) or Lanthanum Carbonate finished formulations upon request. The Lanthanum Carbonate suppliers may include Lanthanum Carbonate API manufacturers, exporters, distributors and traders.
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A Lanthanum Carbonate DMF (Drug Master File) is a document detailing the whole manufacturing process of Lanthanum Carbonate active pharmaceutical ingredient (API) in detail. Different forms of Lanthanum Carbonate DMFs exist exist since differing nations have different regulations, such as Lanthanum Carbonate USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Lanthanum Carbonate DMF submitted to regulatory agencies in the US is known as a USDMF. Lanthanum Carbonate USDMF includes data on Lanthanum Carbonate's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Lanthanum Carbonate USDMF is kept confidential to protect the manufacturer’s intellectual property.
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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 Lanthanum Carbonate Drug Master File in Japan (Lanthanum Carbonate JDMF) empowers Lanthanum Carbonate 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 Lanthanum Carbonate JDMF during the approval evaluation for pharmaceutical products. At the time of Lanthanum Carbonate JDMF registration, PMDA checks if the format is accurate, if the necessary items have been included (application), and if data has been attached.
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In Korea, the Ministry of Food and Drug Safety (MFDS) is in charge of regulating pharmaceutical products and services.
Pharmaceutical companies submit a Lanthanum Carbonate Drug Master File in Korea (Lanthanum Carbonate KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Lanthanum Carbonate. The MFDS reviews the Lanthanum Carbonate KDMF as part of the drug registration process and uses the information provided in the Lanthanum Carbonate KDMF to evaluate the safety and efficacy of the drug.
After submitting a Lanthanum Carbonate KDMF to the MFDS, the registered manufacturer can provide importers or distributors with the registration number without revealing confidential information to Korean business partners. Applicants seeking to register their Lanthanum Carbonate API can apply through the Korea Drug Master File (KDMF).
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A Lanthanum Carbonate written confirmation (Lanthanum Carbonate WC) is an official document issued by a regulatory agency to a Lanthanum Carbonate manufacturer, verifying that the manufacturing facility of a Lanthanum Carbonate active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Lanthanum Carbonate APIs or Lanthanum Carbonate finished pharmaceutical products to another nation, regulatory agencies frequently require a Lanthanum Carbonate WC (written confirmation) as part of the regulatory process.
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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 Lanthanum Carbonate as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Lanthanum Carbonate 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 Lanthanum Carbonate 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 Lanthanum Carbonate and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Lanthanum Carbonate NDC to their finished compounded human drug products, they may choose to do so.
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Lanthanum Carbonate 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 Lanthanum Carbonate 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 Lanthanum Carbonate GMP manufacturer or Lanthanum Carbonate GMP API supplier for your needs.
A Lanthanum Carbonate CoA (Certificate of Analysis) is a formal document that attests to Lanthanum Carbonate's compliance with Lanthanum Carbonate specifications and serves as a tool for batch-level quality control.
Lanthanum Carbonate CoA mostly includes findings from lab analyses of a specific batch. For each Lanthanum Carbonate 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.
Lanthanum Carbonate may be tested according to a variety of international standards, such as European Pharmacopoeia (Lanthanum Carbonate EP), Lanthanum Carbonate JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Lanthanum Carbonate USP).