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